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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251014생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/251014

반응식

참여 물질

역할이름HCID투입량
반응물3-Methylpyridine-2-carboxaldehydeHCID 1501874—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물[4-(1-Thiazol-2-yl-ethylamino)-butyl]-carbamic acid tert-butyl esterHCID 67272661—
용매DichloromethaneHCID 6344—
생성물{4-[(3-Methyl-pyridin-2-ylmethyl)-(1-thiazol-2-yl-ethyl)-amino]-butyl}-carbamic acid tert-butyl esterHCID 67273138—

반응 단계

Using General Procedure B: Reaction of [4-(1-thiazol-2-yl-ethylamino)-butyl]-carbamic acid tert-butyl ester and 3-methyl-2-pyridine carbaldehyde in CH2Cl2 with NaBH(OAc)3 gave {4-[(3-methyl-pyridin-2-ylmethyl)-(1-thiazol-2-yl-ethyl)-amino]-butyl}-carbamic acid tert-butyl ester as an oil. 1H NMR (CDCl3) δ 1.25-1.41 (m, 2H), 1.43 (s, 9H), 1.45-1.53 (m, 2H), 1.55 (d, 3H, J=Hz), 2.47-2.52 (m, 5H), 2.98-3.04 (m, 2H), 3.83 (d, 1H, J=Hz), 4.00 (d, 1H, J=Hz), 4.11 (q, 1H, J=Hz), 4.53 (bs, 1H), 7.10 (dd, 1H, J=7.6, 4.8 Hz), 7.23 (d, 1H, J=3.3 Hz), 7.44 (d, 1H, J=6.8 Hz), 7.66 (d, 1H, J=3.3 Hz), 8.36 (dd, 1H, J=4.8, 1.1 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863293B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-ba3cf5cb877c4251b6c447f9c0d28c5d
출처 메모uspto-grants-2011_01