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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 985230생성일: 2026년 10월 25일

Triethylamine → tert-Butyl (3R)-1-[(7-chlorothieno[3,2-b]pyridin-2-yl)carbonyl]pyrrolidin-3-yl(methyl)carbamate

https://huagongshe.com/reaction/985230

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물tert-Butyl methyl((3R)-pyrrolidin-3-yl)carbamateHCID 7019173—
반응물7-Chlorothieno[3,2-b]pyridine-2-carboxylic acidHCID 11276033—
용매Thionyl ChlorideHCID 24386—
생성물tert-Butyl (3R)-1-[(7-chlorothieno[3,2-b]pyridin-2-yl)carbonyl]pyrrolidin-3-yl(methyl)carbamateHCID 8659075837%

반응 단계

This material was prepared from 7-chlorothieno[3,2-b]pyridine-2-carboxylic acid (1.05 g, 4.94 mmole), SOCl2 (10 ml), tert-butyl methyl[(3R)-pyrrolidin-3-yl]carbamate 34b (0.989 g, 4.94 mmole) and Et3N (0.689 ml, 4.94 mmole) in a manner as previously described for example 9d to give a brown oil (0.723 g, 0.30%). 1H NMR (300 MHz, CDCl3) δ8.62 (1H, d, J=5.1 Hz), 7.85 (1H, s), 7.35 (1H, d, J=5.1 Hz), 4.82 (1H, m), 3.93 (3H, m), 3.63 (1H, m), 2.82 (3H, s), 2.12 (2H, m), 1.47 (9H, s); ESIMS (MH+): 396.05.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06869962B2
출처 데이터셋uspto-grants-2005_03
ORD IDord-556890c459e34648955aeb4eb928cc53
출처 메모uspto-grants-2005_03