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METTLER TOLEDO multigram ii
Multigram Ii, supplied by METTLER TOLEDO, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/multigram+ii/multigram+ii/us11325913-253-11-13
Average 90 stars, based on 1 article reviews
multigram ii - by Bioz Stars, 2026-10
90/100 stars

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Functional Assay:

Article Title: Bicyclic compound and pharmaceutical use thereof
Article Snippet: Trans-tert-butyl{[2-(2-methylpyrazolo[1,5-a]pyridin-4-yl)cyclopropyl]methyl}carbamate (4.80 g) was fractionated by supercritical fluid chromatography (instrument: Multigram II (manufactured by Mettler-Toledo), column: CHIRALPAK AD-HKG-010 (20 mm ID×250 mm L, manufactured by Dicel Chemical Industries, Ltd.), mobile phase: A) carbon dioxide 100%, B) methanol 100%, mixing ratio: A/B=900/100, flow rate: 50 mL/min, column temperature: 35° C., sample concentration: 10 mg/mL (methanol), injection volume: 2.5 mL).

Article Title: Nitrogen-containing five-membered heterocyclic compound
Article Snippet: When the compound has a basic functional group and trifluoroacetic acid is used for this operation, a neutralization operation and the like may be performed to obtain a free form. preparative HPLC instrument: Gilson Inc., High-throughput purification system column: YMC Combiprep ODS-A S-5 μm, 20×50 mm solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=90/10), 1.20 min (SOLUTION A/SOLUTION B=90/10), 4.75 min (SOLUTION A/SOLUTION B=0/100), 7.30 min (SOLUTION A/SOLUTION B=0/100), 7.40 min (SOLUTION A/SOLUTION B=90/10), 7.50 min (SOLUTION A/SOLUTION B=90/10). flow rate: 25 ml/min, detection method: UV 220 nm or tool: Waters mass preparative system (UV Purification System) Column: Develosil ODS-UG-10 solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=95/5), 1.00 min (SOLUTION A/SOLUTION B=95/5), 2.00 min (SOLUTION A/SOLUTION B=80/20), 5.00 min (SOLUTION A/SOLUTION B=5/95), 5.10 min (SOLUTION A/SOLUTION B=0/100), 7.00 min (SOLUTION A/SOLUTION B=100/0) flow rate: 150 ml/min, detection: UV 220 nm In the following Reference Examples and Examples, chiral preparative HPLC was performed using K-Prep manufactured by YMC, and chiral preparation by supercritical fluid chromatography (SFC) was performed using Multigram II manufactured by Mettler Toledo.

Article Title: Indole compound
Article Snippet: In the present specification, the melting point refers to that measured using, for example, micromelting point measuring apparatus (Yanako, MP-500D or Buchi, B-545) or DSC (differential scanning calorimetry) device (SEIKO, EXSTAR6000) and the like.

Neutralization:

Article Title: Bicyclic compound and pharmaceutical use thereof
Article Snippet: Trans-tert-butyl{[2-(2-methylpyrazolo[1,5-a]pyridin-4-yl)cyclopropyl]methyl}carbamate (4.80 g) was fractionated by supercritical fluid chromatography (instrument: Multigram II (manufactured by Mettler-Toledo), column: CHIRALPAK AD-HKG-010 (20 mm ID×250 mm L, manufactured by Dicel Chemical Industries, Ltd.), mobile phase: A) carbon dioxide 100%, B) methanol 100%, mixing ratio: A/B=900/100, flow rate: 50 mL/min, column temperature: 35° C., sample concentration: 10 mg/mL (methanol), injection volume: 2.5 mL).

Article Title: Nitrogen-containing five-membered heterocyclic compound
Article Snippet: When the compound has a basic functional group and trifluoroacetic acid is used for this operation, a neutralization operation and the like may be performed to obtain a free form. preparative HPLC instrument: Gilson Inc., High-throughput purification system column: YMC Combiprep ODS-A S-5 μm, 20×50 mm solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=90/10), 1.20 min (SOLUTION A/SOLUTION B=90/10), 4.75 min (SOLUTION A/SOLUTION B=0/100), 7.30 min (SOLUTION A/SOLUTION B=0/100), 7.40 min (SOLUTION A/SOLUTION B=90/10), 7.50 min (SOLUTION A/SOLUTION B=90/10). flow rate: 25 ml/min, detection method: UV 220 nm or tool: Waters mass preparative system (UV Purification System) Column: Develosil ODS-UG-10 solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=95/5), 1.00 min (SOLUTION A/SOLUTION B=95/5), 2.00 min (SOLUTION A/SOLUTION B=80/20), 5.00 min (SOLUTION A/SOLUTION B=5/95), 5.10 min (SOLUTION A/SOLUTION B=0/100), 7.00 min (SOLUTION A/SOLUTION B=100/0) flow rate: 150 ml/min, detection: UV 220 nm In the following Reference Examples and Examples, chiral preparative HPLC was performed using K-Prep manufactured by YMC, and chiral preparation by supercritical fluid chromatography (SFC) was performed using Multigram II manufactured by Mettler Toledo.

Article Title: Indole compound
Article Snippet: In the present specification, the melting point refers to that measured using, for example, micromelting point measuring apparatus (Yanako, MP-500D or Buchi, B-545) or DSC (differential scanning calorimetry) device (SEIKO, EXSTAR6000) and the like.

High Performance Liquid Chromatography:

Article Title: Bicyclic compound and pharmaceutical use thereof
Article Snippet: Trans-tert-butyl{[2-(2-methylpyrazolo[1,5-a]pyridin-4-yl)cyclopropyl]methyl}carbamate (4.80 g) was fractionated by supercritical fluid chromatography (instrument: Multigram II (manufactured by Mettler-Toledo), column: CHIRALPAK AD-HKG-010 (20 mm ID×250 mm L, manufactured by Dicel Chemical Industries, Ltd.), mobile phase: A) carbon dioxide 100%, B) methanol 100%, mixing ratio: A/B=900/100, flow rate: 50 mL/min, column temperature: 35° C., sample concentration: 10 mg/mL (methanol), injection volume: 2.5 mL).

Article Title: Nitrogen-containing five-membered heterocyclic compound
Article Snippet: When the compound has a basic functional group and trifluoroacetic acid is used for this operation, a neutralization operation and the like may be performed to obtain a free form. preparative HPLC instrument: Gilson Inc., High-throughput purification system column: YMC Combiprep ODS-A S-5 μm, 20×50 mm solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=90/10), 1.20 min (SOLUTION A/SOLUTION B=90/10), 4.75 min (SOLUTION A/SOLUTION B=0/100), 7.30 min (SOLUTION A/SOLUTION B=0/100), 7.40 min (SOLUTION A/SOLUTION B=90/10), 7.50 min (SOLUTION A/SOLUTION B=90/10). flow rate: 25 ml/min, detection method: UV 220 nm or tool: Waters mass preparative system (UV Purification System) Column: Develosil ODS-UG-10 solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=95/5), 1.00 min (SOLUTION A/SOLUTION B=95/5), 2.00 min (SOLUTION A/SOLUTION B=80/20), 5.00 min (SOLUTION A/SOLUTION B=5/95), 5.10 min (SOLUTION A/SOLUTION B=0/100), 7.00 min (SOLUTION A/SOLUTION B=100/0) flow rate: 150 ml/min, detection: UV 220 nm In the following Reference Examples and Examples, chiral preparative HPLC was performed using K-Prep manufactured by YMC, and chiral preparation by supercritical fluid chromatography (SFC) was performed using Multigram II manufactured by Mettler Toledo.

Article Title: Indole compound
Article Snippet: In the present specification, the melting point refers to that measured using, for example, micromelting point measuring apparatus (Yanako, MP-500D or Buchi, B-545) or DSC (differential scanning calorimetry) device (SEIKO, EXSTAR6000) and the like.

Purification:

Article Title: Bicyclic compound and pharmaceutical use thereof
Article Snippet: Trans-tert-butyl{[2-(2-methylpyrazolo[1,5-a]pyridin-4-yl)cyclopropyl]methyl}carbamate (4.80 g) was fractionated by supercritical fluid chromatography (instrument: Multigram II (manufactured by Mettler-Toledo), column: CHIRALPAK AD-HKG-010 (20 mm ID×250 mm L, manufactured by Dicel Chemical Industries, Ltd.), mobile phase: A) carbon dioxide 100%, B) methanol 100%, mixing ratio: A/B=900/100, flow rate: 50 mL/min, column temperature: 35° C., sample concentration: 10 mg/mL (methanol), injection volume: 2.5 mL).

Article Title: Nitrogen-containing five-membered heterocyclic compound
Article Snippet: When the compound has a basic functional group and trifluoroacetic acid is used for this operation, a neutralization operation and the like may be performed to obtain a free form. preparative HPLC instrument: Gilson Inc., High-throughput purification system column: YMC Combiprep ODS-A S-5 μm, 20×50 mm solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=90/10), 1.20 min (SOLUTION A/SOLUTION B=90/10), 4.75 min (SOLUTION A/SOLUTION B=0/100), 7.30 min (SOLUTION A/SOLUTION B=0/100), 7.40 min (SOLUTION A/SOLUTION B=90/10), 7.50 min (SOLUTION A/SOLUTION B=90/10). flow rate: 25 ml/min, detection method: UV 220 nm or tool: Waters mass preparative system (UV Purification System) Column: Develosil ODS-UG-10 solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=95/5), 1.00 min (SOLUTION A/SOLUTION B=95/5), 2.00 min (SOLUTION A/SOLUTION B=80/20), 5.00 min (SOLUTION A/SOLUTION B=5/95), 5.10 min (SOLUTION A/SOLUTION B=0/100), 7.00 min (SOLUTION A/SOLUTION B=100/0) flow rate: 150 ml/min, detection: UV 220 nm In the following Reference Examples and Examples, chiral preparative HPLC was performed using K-Prep manufactured by YMC, and chiral preparation by supercritical fluid chromatography (SFC) was performed using Multigram II manufactured by Mettler Toledo.

Article Title: Indole compound
Article Snippet: In the present specification, the melting point refers to that measured using, for example, micromelting point measuring apparatus (Yanako, MP-500D or Buchi, B-545) or DSC (differential scanning calorimetry) device (SEIKO, EXSTAR6000) and the like.

Solvent:

Article Title: Bicyclic compound and pharmaceutical use thereof
Article Snippet: Trans-tert-butyl{[2-(2-methylpyrazolo[1,5-a]pyridin-4-yl)cyclopropyl]methyl}carbamate (4.80 g) was fractionated by supercritical fluid chromatography (instrument: Multigram II (manufactured by Mettler-Toledo), column: CHIRALPAK AD-HKG-010 (20 mm ID×250 mm L, manufactured by Dicel Chemical Industries, Ltd.), mobile phase: A) carbon dioxide 100%, B) methanol 100%, mixing ratio: A/B=900/100, flow rate: 50 mL/min, column temperature: 35° C., sample concentration: 10 mg/mL (methanol), injection volume: 2.5 mL).

Article Title: Nitrogen-containing five-membered heterocyclic compound
Article Snippet: When the compound has a basic functional group and trifluoroacetic acid is used for this operation, a neutralization operation and the like may be performed to obtain a free form. preparative HPLC instrument: Gilson Inc., High-throughput purification system column: YMC Combiprep ODS-A S-5 μm, 20×50 mm solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=90/10), 1.20 min (SOLUTION A/SOLUTION B=90/10), 4.75 min (SOLUTION A/SOLUTION B=0/100), 7.30 min (SOLUTION A/SOLUTION B=0/100), 7.40 min (SOLUTION A/SOLUTION B=90/10), 7.50 min (SOLUTION A/SOLUTION B=90/10). flow rate: 25 ml/min, detection method: UV 220 nm or tool: Waters mass preparative system (UV Purification System) Column: Develosil ODS-UG-10 solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=95/5), 1.00 min (SOLUTION A/SOLUTION B=95/5), 2.00 min (SOLUTION A/SOLUTION B=80/20), 5.00 min (SOLUTION A/SOLUTION B=5/95), 5.10 min (SOLUTION A/SOLUTION B=0/100), 7.00 min (SOLUTION A/SOLUTION B=100/0) flow rate: 150 ml/min, detection: UV 220 nm In the following Reference Examples and Examples, chiral preparative HPLC was performed using K-Prep manufactured by YMC, and chiral preparation by supercritical fluid chromatography (SFC) was performed using Multigram II manufactured by Mettler Toledo.

Article Title: Indole compound
Article Snippet: In the present specification, the melting point refers to that measured using, for example, micromelting point measuring apparatus (Yanako, MP-500D or Buchi, B-545) or DSC (differential scanning calorimetry) device (SEIKO, EXSTAR6000) and the like.

Supercritical Fluid Chromatography:

Article Title: Bicyclic compound and pharmaceutical use thereof
Article Snippet: Trans-tert-butyl{[2-(2-methylpyrazolo[1,5-a]pyridin-4-yl)cyclopropyl]methyl}carbamate (4.80 g) was fractionated by supercritical fluid chromatography (instrument: Multigram II (manufactured by Mettler-Toledo), column: CHIRALPAK AD-HKG-010 (20 mm ID×250 mm L, manufactured by Dicel Chemical Industries, Ltd.), mobile phase: A) carbon dioxide 100%, B) methanol 100%, mixing ratio: A/B=900/100, flow rate: 50 mL/min, column temperature: 35° C., sample concentration: 10 mg/mL (methanol), injection volume: 2.5 mL).

Article Title: Nitrogen-containing five-membered heterocyclic compound
Article Snippet: When the compound has a basic functional group and trifluoroacetic acid is used for this operation, a neutralization operation and the like may be performed to obtain a free form. preparative HPLC instrument: Gilson Inc., High-throughput purification system column: YMC Combiprep ODS-A S-5 μm, 20×50 mm solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=90/10), 1.20 min (SOLUTION A/SOLUTION B=90/10), 4.75 min (SOLUTION A/SOLUTION B=0/100), 7.30 min (SOLUTION A/SOLUTION B=0/100), 7.40 min (SOLUTION A/SOLUTION B=90/10), 7.50 min (SOLUTION A/SOLUTION B=90/10). flow rate: 25 ml/min, detection method: UV 220 nm or tool: Waters mass preparative system (UV Purification System) Column: Develosil ODS-UG-10 solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=95/5), 1.00 min (SOLUTION A/SOLUTION B=95/5), 2.00 min (SOLUTION A/SOLUTION B=80/20), 5.00 min (SOLUTION A/SOLUTION B=5/95), 5.10 min (SOLUTION A/SOLUTION B=0/100), 7.00 min (SOLUTION A/SOLUTION B=100/0) flow rate: 150 ml/min, detection: UV 220 nm In the following Reference Examples and Examples, chiral preparative HPLC was performed using K-Prep manufactured by YMC, and chiral preparation by supercritical fluid chromatography (SFC) was performed using Multigram II manufactured by Mettler Toledo.

Article Title: Indole compound
Article Snippet: In the present specification, the melting point refers to that measured using, for example, micromelting point measuring apparatus (Yanako, MP-500D or Buchi, B-545) or DSC (differential scanning calorimetry) device (SEIKO, EXSTAR6000) and the like.

Concentration Assay:

Article Title: Bicyclic compound and pharmaceutical use thereof
Article Snippet: Trans-tert-butyl{[2-(2-methylpyrazolo[1,5-a]pyridin-4-yl)cyclopropyl]methyl}carbamate (4.80 g) was fractionated by supercritical fluid chromatography (instrument: Multigram II (manufactured by Mettler-Toledo), column: CHIRALPAK AD-HKG-010 (20 mm ID×250 mm L, manufactured by Dicel Chemical Industries, Ltd.), mobile phase: A) carbon dioxide 100%, B) methanol 100%, mixing ratio: A/B=900/100, flow rate: 50 mL/min, column temperature: 35° C., sample concentration: 10 mg/mL (methanol), injection volume: 2.5 mL).

Article Title: Nitrogen-containing five-membered heterocyclic compound
Article Snippet: When the compound has a basic functional group and trifluoroacetic acid is used for this operation, a neutralization operation and the like may be performed to obtain a free form. preparative HPLC instrument: Gilson Inc., High-throughput purification system column: YMC Combiprep ODS-A S-5 μm, 20×50 mm solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=90/10), 1.20 min (SOLUTION A/SOLUTION B=90/10), 4.75 min (SOLUTION A/SOLUTION B=0/100), 7.30 min (SOLUTION A/SOLUTION B=0/100), 7.40 min (SOLUTION A/SOLUTION B=90/10), 7.50 min (SOLUTION A/SOLUTION B=90/10). flow rate: 25 ml/min, detection method: UV 220 nm or tool: Waters mass preparative system (UV Purification System) Column: Develosil ODS-UG-10 solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=95/5), 1.00 min (SOLUTION A/SOLUTION B=95/5), 2.00 min (SOLUTION A/SOLUTION B=80/20), 5.00 min (SOLUTION A/SOLUTION B=5/95), 5.10 min (SOLUTION A/SOLUTION B=0/100), 7.00 min (SOLUTION A/SOLUTION B=100/0) flow rate: 150 ml/min, detection: UV 220 nm In the following Reference Examples and Examples, chiral preparative HPLC was performed using K-Prep manufactured by YMC, and chiral preparation by supercritical fluid chromatography (SFC) was performed using Multigram II manufactured by Mettler Toledo.

Article Title: Indole compound
Article Snippet: In the present specification, the melting point refers to that measured using, for example, micromelting point measuring apparatus (Yanako, MP-500D or Buchi, B-545) or DSC (differential scanning calorimetry) device (SEIKO, EXSTAR6000) and the like.

Injection:

Article Title: Bicyclic compound and pharmaceutical use thereof
Article Snippet: Trans-tert-butyl{[2-(2-methylpyrazolo[1,5-a]pyridin-4-yl)cyclopropyl]methyl}carbamate (4.80 g) was fractionated by supercritical fluid chromatography (instrument: Multigram II (manufactured by Mettler-Toledo), column: CHIRALPAK AD-HKG-010 (20 mm ID×250 mm L, manufactured by Dicel Chemical Industries, Ltd.), mobile phase: A) carbon dioxide 100%, B) methanol 100%, mixing ratio: A/B=900/100, flow rate: 50 mL/min, column temperature: 35° C., sample concentration: 10 mg/mL (methanol), injection volume: 2.5 mL).

Article Title: Nitrogen-containing five-membered heterocyclic compound
Article Snippet: When the compound has a basic functional group and trifluoroacetic acid is used for this operation, a neutralization operation and the like may be performed to obtain a free form. preparative HPLC instrument: Gilson Inc., High-throughput purification system column: YMC Combiprep ODS-A S-5 μm, 20×50 mm solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=90/10), 1.20 min (SOLUTION A/SOLUTION B=90/10), 4.75 min (SOLUTION A/SOLUTION B=0/100), 7.30 min (SOLUTION A/SOLUTION B=0/100), 7.40 min (SOLUTION A/SOLUTION B=90/10), 7.50 min (SOLUTION A/SOLUTION B=90/10). flow rate: 25 ml/min, detection method: UV 220 nm or tool: Waters mass preparative system (UV Purification System) Column: Develosil ODS-UG-10 solvent: SOLUTION A; 0.1% trifluoroacetic acid-containing water, SOLUTION B; 0.1% trifluoroacetic acid-containing acetonitrile gradient cycle: 0.00 min (SOLUTION A/SOLUTION B=95/5), 1.00 min (SOLUTION A/SOLUTION B=95/5), 2.00 min (SOLUTION A/SOLUTION B=80/20), 5.00 min (SOLUTION A/SOLUTION B=5/95), 5.10 min (SOLUTION A/SOLUTION B=0/100), 7.00 min (SOLUTION A/SOLUTION B=100/0) flow rate: 150 ml/min, detection: UV 220 nm In the following Reference Examples and Examples, chiral preparative HPLC was performed using K-Prep manufactured by YMC, and chiral preparation by supercritical fluid chromatography (SFC) was performed using Multigram II manufactured by Mettler Toledo.

Article Title: Indole compound
Article Snippet: In the present specification, the melting point refers to that measured using, for example, micromelting point measuring apparatus (Yanako, MP-500D or Buchi, B-545) or DSC (differential scanning calorimetry) device (SEIKO, EXSTAR6000) and the like.



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