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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296941Generated: October 30, 2026

4-Nitrobenzoyl chloride → N-{4-[2-cyclopentyl-1-(thiazol-2-ylcarbamoyl)-ethyl]-phenyl}-4-nitro-benzamide

https://huagongshe.com/reaction/2296941

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(4-amino-phenyl)-3-cyclopentyl-N-thiazol-2-yl-propionamideHCID 9948802—
SolventTetrahydrofuranHCID 8028—
ProductN-{4-[2-cyclopentyl-1-(thiazol-2-ylcarbamoyl)-ethyl]-phenyl}-4-nitro-benzamideHCID 989063379.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-(4-amino-phenyl)-3-cyclopentyl-N-thiazol-2-yl-propionamide (prepared in Example 3, 63.0 mg, 0.20 mmol) in tetrahydrofuran (10 mL) was treated with N,N-diisopropylethylamine (0.04 mL, 0.24 mmol) and 4-nitro-benzoyl chloride (49.0 mg, 0.26 mmol). The reaction mixture was stirred at 25° C. for 21 h. At this time, the reaction was concentrated in vacuo. The residue was triturated with diethyl ether to afford N-{4-[2-cyclopentyl-1-(thiazol-2-ylcarbamoyl)-ethyl]-phenyl}-4-nitro-benzamide (73.7 mg, 79.3%) as a pale yellow solid: mp 236-238° C.; FAB-HRMS m/e calcd for C24H24N4O4S (M+H)+ 465.1596, found 465.1617.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489485B2
Source datasetuspto-grants-2002_12
ORD IDord-3477d41943c943efa216a409f84f7a0f
Source noteuspto-grants-2002_12