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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968773Generated: October 29, 2026

HCID 178430969, compound → HCID 178430523, compound

https://huagongshe.com/reaction/968773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178430969HCID 178430969—
ReactantHCID 178430970HCID 178430970—
ProductHCID 178430523HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304084B2
Source datasetuspto-grants-2007_12
ORD IDord-a33801b3311d4d11bf91fcead776bb26
Source noteuspto-grants-2007_12