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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63131생성일: 2026년 10월 23일

2,3-Dimethylcyclohexylamine → N4-(2,3-dimethylcyclohexyl)-5,6-dimethyl-N2-(pyridin-2-ylmethyl)pyrimidine-2,4-diamine

https://huagongshe.com/ko/reaction/63131

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참여 물질

역할이름HCID투입량
반응물2,3-DimethylcyclohexylamineHCID 123507—
반응물N4-cyclopentyl-5,6-dimethyl-N2-(pyridin-2-ylmethyl)pyrimidine-2,4-diamineHCID 71738410—
생성물N4-(2,3-dimethylcyclohexyl)-5,6-dimethyl-N2-(pyridin-2-ylmethyl)pyrimidine-2,4-diamineHCID 71738549—

반응 단계

The titled compound was synthesized according to the procedure described for preparation of N4-cyclopentyl-5,6-dimethyl-N2-(pyridin-2-ylmethyl)pyrimidine-2,4-diamine (Example 29) using 2,3-dimethylcyclohexanamine instead of cyclopentanamine. The crude material was purified by column chromatography eluting with mixture of chloroform/ethanol/20% water solution of ammonia (200:10:1), and then the final product was washed with diethyl ether to afford the titled compound as a white solid. 1H NMR (400 MHz, CDCl3) δ ppm 0.75-0.76 (m, 3H), 0.85-0.95 (m, 3H), 1.55-1.74 (m, 8H), 1.86-1.97 (m, 4H), 2.07 (s, 3H), 3.10-3.18 (m, 1H), 4.43 (bs, 2H), 7.20-7.26 (m, 1H), 7.50-7.57 (m, 1H), 7.67-7.73 (m, 1H), 8.60-7.68 (m, 1H); MS (ESI) m/z 340.4 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447051B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-3c7d12f4818d46aa9a3ddfe851cb3294
출처 메모uspto-grants-2016_09