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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966851Generated: October 26, 2026

Triethylamine → 3-cyclopentyl-2-(4-methanesulfonyl-3-nitro-phenyl)-N-pyrimidin-4-yl-propionamide

https://huagongshe.com/reaction/966851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-AminopyrimidineHCID 68958—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant3-Cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-propionic acidHCID 12010541—
SolventDichloromethaneHCID 6344—
Product3-cyclopentyl-2-(4-methanesulfonyl-3-nitro-phenyl)-N-pyrimidin-4-yl-propionamideHCID 2231521230.5%

Reaction Steps

A solution of 3-cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-propionic acid (prepared as in Example 14, 150 mg, 0.439 mmol), triethylamine (0.184 mL, 1.32 mmol), benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (291 mg, 0.659 mmol), and 4-aminopyrimidine (63 mg, 0.659 mmol) in methylene chloride (4 mL) was stirred at 25° C. overnight. The crude reaction mixture was directly purified by Biotage chromatography (FLASH 40M, Silica, 1/2 hexanes/ethyl acetate) to afford 3-cyclopentyl-2-(4-methanesulfonyl-3-nitro-phenyl)-N-pyrimidin-4-yl-propionamide (56 mg, 30%) as a pale yellow foam: mp 91-95° C. (foam to gel); EI-HRMS m/e calcd for C19H22N4O5S (M+) 418.1311, found 418.1310.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951945B2
Source datasetuspto-grants-2005_10
ORD IDord-565bef8c68254da5937ab6b24dad0bb6
Source noteuspto-grants-2005_10