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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2386387생성일: 2026년 10월 26일

Methanesulfonyl chloride → 4-{[3-(2-Chloro-pyrimidin-4-yl)-benzyl]-methanesulfonyl-amino}-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2386387

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물4-[3-(2-Chloro-pyrimidin-4-yl)-benzylamino]-piperidine-1-carboxylic acid tert-butyl esterHCID 86603263—
생성물4-{[3-(2-Chloro-pyrimidin-4-yl)-benzyl]-methanesulfonyl-amino}-piperidine-1-carboxylic acid tert-butyl esterHCID 86603264—

반응 단계

Intermediate 29 was coupled with methanesulfonyl chloride following procedure D. LC-MS showed the product had the expected M+H+ of 481. 1H NMR (Varian 300 MHz, CD3OD, shifts relative to the solvent peak at 3.3 ppm) δ 8.4 (s, 1H) 8.39 (d, 1H) 8.2 (d, 1H) 7.6 (d, 1H) 7.5 (s, 1H), 7.3 (m, 3H), 7.0 (d, 1H), 6.9 (d 1H), 6.8 (d, 2H), 6.5 (d, 2H), 4.6 (s, 2H), 3.6 (m, 4H), 2.8 (t, 2H), 1.2 (d, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08268822B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-94b7cefaecfa43fbb438dac60fc551f7
출처 메모uspto-grants-2012_09