HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910122Generated: October 31, 2026
Isoquinoline-3-carboxylic acid → HCID 66940229, compound
https://huagongshe.com/reaction/1910122
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isoquinoline-3-carboxylic acid | HCID 124656 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | HCID 58190839 | HCID 58190839 | — |
| Product | HCID 66940229 | HCID 66940229 | 80.8% |
Reaction Steps
0.5 g (2.12 mmol) of 2-amino-6-nitro-1H-benzoimidazole-4-carboxylic acid methyl ester was reacted with 0.37 g (2.12 mmol) of isoquinoline 3-carboxylic acid and 0.89 g (2.33 mmol) of HBTU as described in general procedure A to provide 0.67 g (80%) of 2-[(Isoquinoline-3-carbonyl)-amino]-6-nitro-1H-benzoimidazole-4-carboxylic acid methyl ester. LCMS: 392 (M+1)+. The ester was dissolved in dry DMF (5 mL) and 0.22 g (5.1 mmol) of LiCl in one portion was added. The resulting mixture was stirred at 120° C. for 12 h, diluted with water, and the solid was collected by filtration. The solid was washed with water (20 mL), ether (10 mL) and dried under vacuum to provide 0.6 g (93%) of 2-[(isoquinoline-3-carbonyl)-amino]-6-nitro-1H-benzoimidazole-4-carboxylic acid. LCMS: 378 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598353B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-e72c2f2e651641b6be7fbb78bcad53b5 |
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| Source note | uspto-grants-2013_12 |
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