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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20831생성일: 2026년 10월 25일

Dicyclohexylcarbodiimide → N-[[1-(Dimethylamino)cyclopentyl](phenyl)methyl]-2-methyl-6-(methyloxy)benzamide

https://huagongshe.com/reaction/20831

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2-Methoxy-6-methylbenzoic acidHCID 273170—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물{1-[Amino(phenyl)methyl]cyclopentyl}dimethylamineHCID 11521393—
반응물2-Chloro-N-[[1-(dimethylamino)cyclopentyl](phenyl)methyl]-3-(trifluoromethyl)benzamideHCID 11611585—
용매DichloromethaneHCID 6344—
생성물N-[[1-(Dimethylamino)cyclopentyl](phenyl)methyl]-2-methyl-6-(methyloxy)benzamideHCID 11588687—

반응 단계

A mixture of {1-[amino(phenyl)methyl]cyclopentyl}dimethylamine D3 enantiomer 2 (0.220 g, 1 mmol), 2-methoxy-6-methylbenzoic acid (0.200 g, 1.2 mmol), 1-hydroxybenzotriazole hydrate (0.183 g, 1.2 mmol) and PS-DCC (1 g of 1.3 mmol/g loading, 1.3 mmol) in DCM (10 ml) was stirred vigorously overnight. The mixture was washed with saturated aqueous sodium hydrogen carbonate, the layers separated through a phase separation cartridge and the organic layer applied to an SCX cartridge. The cartridge was eluted with DCM (×2), and then methanol (×2) followed by 1M ammonia in methanol. Evaporation of the solvent afforded the title compound which was characterised. 1H NMR (CDCl3) δ: 1.00-1.10 (1H, m), 1.25-1.40 (1H, m), 1.40-1.60 (2H, m), 1.60-1.80 (2H, m), 1.80-2.00 (2H, m), 2.24 (6H, s), 2.28 (3H, s), 3.80 (3H, s), 5.17 (1H, d, J=6 Hz), 6.75 (1H, d, J=8 Hz), 6.79 (1H, d, J=8 Hz), 7.10 (1H, br s), 7.15-7.30 (4H, m), 7.44 (2H, m). Mass Spectrum (Electrospray LC/MS): Found 367 (MH+). C23H30N2O2 requires 366. Ret. time 1.92 min. The title product was converted to the corresponding hydrochloride salt (0.34 g, 85%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745642B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-fdd1e5fac5a841df87c2ae73df0cbf53
출처 메모uspto-grants-2010_06