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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 540121생성일: 2026년 10월 26일

tert-butyl N-(pyrrolidin-3-yl)carbamate → 1-[6-Methyl-2-(1-oxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)quinolin-4-yl]pyrrolidin-3-amine

https://huagongshe.com/reaction/540121

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl N-(pyrrolidin-3-yl)carbamateHCID 2757234—
반응물4-(4-Chloro-6-methylquinolin-2-yl)-2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxideHCID 71255379—
생성물1-[6-Methyl-2-(1-oxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)quinolin-4-yl]pyrrolidin-3-amineHCID 71262210—

반응 단계

The title compound was prepared in analogy to Example 19-1 in Scheme 7 by using 4-(4-chloro-6-methylquinolin-2-yl)-2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxide (prepared in analogy to the one in Example 18-1) and tert-butyl pyrrolidin-3-ylcarbamate. MS obsd. (ESI+) [(M+H)+] 407, 1H NMR (400 MHz, CD3OD) δ ppm 7.81 (s, 1 H), 7.71 (t, J=8.21 Hz, 2 H), 7.57-7.36 (m, 3 H), 7.27 (dd, J=8.59, 1.77 Hz, 1 H), 6.11 (s, 1 H), 5.21 (d, J=16.17 Hz, 1 H), 4.76 (d, J=15.92 Hz, 2 H), 4.50 (brs, 1 H), 3.88-3.71 (m, 2 H), 3.71-3.53 (m, 2 H), 3.53-3.36 (m, 3 H), 2.40 (s, 3 H), 2.26 (dq, J=12.63, 6.23 Hz, 1 H), 1.98-1.78 (m, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871756B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-6770b24e88234cfc9d65eff4774b330f
출처 메모uspto-grants-2014_10