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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382373Generated: October 30, 2026

Benzoyl chloride → HCID 18360248, compound

https://huagongshe.com/reaction/382373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant2-Methoxybenzoyl chlorideHCID 88969—
Reactant1-benzyl-4-amino-1H-imidazole-5-carboxamideHCID 14000620—
ProductHCID 18360248HCID 1836024853%

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 2-methoxybenzoyl chloride separately prepared according to a conventional method, instead of benzoyl chloride, to obtain a crude amide product. The crude amide product was purified by suspension in hot methanol to obtain 1.87 g of 4-(2-methoxybenzoylamino)-1-benzyl-5-imidazolecarboxamide (yield 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310070B1
Source datasetuspto-grants-2001_10
ORD IDord-10ce8324736a4f258f24ac2d1c5d5c1a
Source noteuspto-grants-2001_10