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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20844생성일: 2026년 10월 24일

2,6-Dimethylbenzoic acid → 2,6-Dimethyl-N-[[1-(methylamino)cyclopentyl](phenyl)methyl]benzamide

https://huagongshe.com/ko/reaction/20844

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Dimethylbenzoic acidHCID 12439—
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—
생성물2,6-Dimethyl-N-[[1-(methylamino)cyclopentyl](phenyl)methyl]benzamideHCID 1152288676%

반응 단계

To a solution of 2,6-dimethylbenzoic acid (0.100 g; 0.668 mmol) in DMF (5 ml) and DIPEA (0.12 ml) was added {[amino(phenyl)methyl]cyclopentyl}methylamine D31 enantiomer 2 (0.124 g; 0.608 mmol) and HATU (0.254 g; 0.668 mmol). The resulting mixture was allowed to stir at room temperature for 3 days and then the DMF was evaporated off under reduced pressure. Residual material was partitioned between ethyl acetate and water, washed with water and the organic layer was dried (Na2SO4) and evaporated. The residual material was dissolved in DCM (2 ml) and loaded onto an SCX cartridge. Washing with DCM, then methanol followed by elution with 1 M ammonia in methanol afforded the title product (155 mg; 76%). 1H NMR (CDCl3) δ: 1.3-1.8 (9H, m), 2.21 (3H, s), 2.28 (6H, s), 5.07 (1H, m), 7.0 (2H, m), 7.1-7.4 (7H, m). Mass Spectrum (Electrospray LC/MS). Found 337 (MH+). C22H28N2O requires 336. Ret. time: 1.86 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745642B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-4d7b6c3ca3c241229878f9f0254ed117
출처 메모uspto-grants-2010_06