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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300945Generated: October 30, 2026

2-amino-N-(4-chlorophenyl)-5-methylbenzamide → Benzo[b]thiophene-2-carboxamide, 3-chloro-N-[2-[[(4-chlorophenyl)amino]carbonyl]-4-methylphenyl]-

https://huagongshe.com/reaction/2300945

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-amino-N-(4-chlorophenyl)-5-methylbenzamideHCID 335170—
Reactant3-Chlorobenzo(b)thiophene-2-carbonyl chlorideHCID 519898—
SolventPyridineHCID 1049—
ProductBenzo[b]thiophene-2-carboxamide, 3-chloro-N-[2-[[(4-chlorophenyl)amino]carbonyl]-4-methylphenyl]-HCID 1041168450%

Reaction Steps

To a solution of N-(4-chlorophenyl)-2-amino-5-methylbenzamide (0.11 g, 0.42 mmol) in pyridine (5 mL) at 0° C. was added 2-chlorocarbonyl-3-chlorobenzo[b]thiophene (0.15 g, 0.64 mmol), and the mixture allowed to warm to ambient temperature with stirring. After 16 hours, the mixture was poured onto water (5 mL) and the resulting white solid collected by filtration and dried in vacuo. Recrystallization from acetonitrile afforded 0.095 g (50% yield) of N-(4-chlorophenyl)-2-[((3-chlorobenzo[b]thien-2-yl)carbonyl)amino]-5-methylbenzamide, as a white crystalline solid; NMR (DMSO-d6/TFA) 11.4 (s, 1), 10.7 (s, 1), 8.2 (d, 1), 7.4-8.2 (m, 10), 2.4 (s, 3) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498185B1
Source datasetuspto-grants-2002_12
ORD IDord-10c50ae4f00d4e1aa5e48f6a64142feb
Source noteuspto-grants-2002_12