HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968773Generated: October 29, 2026
HCID 178430969, compound → HCID 178430523, compound
https://huagongshe.com/reaction/968773
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178430969 | HCID 178430969 | — |
| Reactant | HCID 178430970 | HCID 178430970 | — |
| Product | HCID 178430523 | HCID 178430523 | — |
Reaction Steps
As to General Reaction Scheme 3, intermediate (22) (produced via, inter alia, General Scheme 2) is nitrated by a nitrating agent to yield intermediate 7-Methyl-6-nitro-1H-benzimidazole-4-carboxylic acid (23). In turn, intermediate (23) may either be amidated/dehydrated by an amidating/dehydrating agent to yield intermediate 7-Methyl-6-nitro-1H-benzimidazole-4-carbonitrile (24), or amidated by an amidating agent to yield intermediate 7-Methyl-6-nitro-1H-benzimidazole-4-carboxamide (25). Intermediate (24) is reduced by a nitro group reducing agent to yield intermediate (10). In turn, intermediate (25) is reduced by a nitro group reducing agent to yield intermediate 6-Amino-7-methyl-1H-benzimidazole-4-carboxamide, hydrochloric acid salt (26), and thereafter dehydrated by an amide dehydrating agent to yield intermediate (10). See Examples 13 and 14.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07304084B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-a33801b3311d4d11bf91fcead776bb26 |
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| Source note | uspto-grants-2007_12 |
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