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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251016생성일: 2026년 10월 26일

3-Methylpyridine-2-carboxaldehyde → {4-[(3-Methyl-pyridin-2-ylmethyl)-(1-pyrazin-2-yl-ethyl)-amino]-butyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/251016

반응식

참여 물질

역할이름HCID투입량
반응물3-Methylpyridine-2-carboxaldehydeHCID 1501874—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물[4-(1-Pyrazin-2-yl-ethylamino)-butyl]-carbamic acid tert-butyl esterHCID 67272616—
용매DichloromethaneHCID 6344—
생성물{4-[(3-Methyl-pyridin-2-ylmethyl)-(1-pyrazin-2-yl-ethyl)-amino]-butyl}-carbamic acid tert-butyl esterHCID 6727240563%

반응 단계

Using General Procedure B: Reaction of [4-(1-pyrazin-2-yl-ethylamino)-butyl]-carbamic acid tert-butyl ester and 3-methyl-pyridine-2-carbaldehyde in CH2Cl2 with NaBH(OAc)3 gave {4-[(3-methyl-pyridin-2-ylmethyl)-(1-pyrazin-2-yl-ethyl)-amino]-butyl}-carbamic acid tert-butyl ester (229 m, 63%) as an oil. 1H NMR (CDCl3) δ 1.26-1.39 (m, 6H), 1.43 (s, 9H), 1.50 (d, 1H, J=7.0 Hz), 2.30 (s, 3H), 2.90-2.96 (m, 2H), 4.05 (s, 2H), 4.08 (d, 1H, J=7.0 Hz) 7.10 (dd, 1H, J=7.5, 4.8 Hz), 7.41 (d, 1H, J=7.5 Hz), 8.37 (dd, 1H, J=5.1, 1.2 Hz), 8.39 (s, 1H), 8.48-8.50 (m, 1H), 8.63 (d, 1H, J=1.5 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863293B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-7ef848e795cc4a06824628fe7c738d06
출처 메모uspto-grants-2011_01