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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20842생성일: 2026년 10월 24일

2-Chloro-3-(trifluoromethyl)benzoic acid → (+/-)-2-Chloro-N-[[1-(methylamino)cyclopentyl](phenyl)methyl]-3-(trifluoromethyl)benzamide

https://huagongshe.com/ko/reaction/20842

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-3-(trifluoromethyl)benzoic acidHCID 2736677—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물{[Amino(phenyl)methyl]cyclopentyl}methylamineHCID 57444874—
용매DimethylformamideHCID 6228—
용매DiisopropylethylamineHCID 81531—
생성물(+/-)-2-Chloro-N-[[1-(methylamino)cyclopentyl](phenyl)methyl]-3-(trifluoromethyl)benzamideHCID 59347824—

반응 단계

To a solution of 2-chloro-3-(trifluoromethyl)benzoic acid (0.728 g; 3.24 mmol) in DMF (20 ml) and DIPEA (2.5 ml) was added (±)-{[amino(phenyl)methyl]cyclopentyl}methylamine D29 (1.0 g; 3.60 mmol) and HATU (1.23 g; 3.24 mmol). The resulting mixture was allowed to stir at room temperature overnight and then DMF evaporated off in vacuo. Residual material was partitioned between ethyl acetate and water. The organic layer was dried (Na2SO4) and the filtrate evaporated in vacuo. The desired product was isolated by column chromatography on silica gel using 20% diethyl ether to 100% diethyl ether in n-pentane to afford the title compound as a white solid (0.908 g; 61%). 1H NMR (CDCl3) δ: 1.47-1.83 (9H, m), 2.21 (3H, s), 5.1 (1H, m), 7.23-7.43 (6H, m), 7.58 (1H, m), 7.65 (1H, m), 7.73 (1H, m); Mass Spectrum (Electrospray LC/MS), API+: Found 411 (MH+). C21H2235ClF3N2O requires 410. Ret. time 2.04 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745642B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-52e008b438bc49e8b5555b7bdf07b14c
출처 메모uspto-grants-2010_06