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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382374Generated: October 31, 2026

m-Anisoyl chloride → HCID 18360431, compound

https://huagongshe.com/reaction/382374

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Anisoyl chlorideHCID 74374—
Reactant2-benzoylbenzoyl chlorideHCID 10999295—
Reactant1-benzyl-4-amino-1H-imidazole-5-carboxamideHCID 14000620—
ProductHCID 18360431HCID 1836043126%

Reaction Steps

An amidation reaction and post-treatment were carried out according to the conditions of Example 1, using 2.2 g (10 mmol) of 4-amino-1-benzyl-5-imidazolecarboxamide prepared in Reference Example 2 and 3-methoxybenzoyl chloride separately prepared according to a conventional method, instead of benzoyl benzoyl chloride, to obtain a crude amide product. The crude amide product was purified by suspension in hot methanol to obtain 0.91 g of 4-(3-methoxybenzoylamino)-1-benzyl-5-imidazolecarboxamide (yield 26%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310070B1
Source datasetuspto-grants-2001_10
ORD IDord-11f61b72f10e4504a4b26bf2415590e1
Source noteuspto-grants-2001_10