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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370115Generated: October 31, 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/370115

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 numberUS06140351
Source datasetuspto-grants-2000_10
ORD IDord-3c8a4d0cc0714af8a90870afe22e5c6c
Source noteuspto-grants-2000_10