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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844185Generated: 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/844185

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 numberUS06380221B1
Source datasetuspto-grants-2002_04
ORD IDord-33cbd5dee59a44be8731010a5c7904ab
Source noteuspto-grants-2002_04