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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30413생성일: 2026년 10월 24일

1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine → 4-[4-Fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/30413

반응식

참여 물질

역할이름HCID투입량
반응물1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
반응물BEMP resinHCID 16216994—
반응물4-[1-(4-chloro-phenyl)-1H-indazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl esterHCID 68530176—
반응물HCID 178518865HCID 178518865—
용매DimethylformamideHCID 6228—
생성물4-[4-Fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl esterHCID 6853283651%

반응 단계

4-[4-Fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 46) was prepared as described above for Intermediate 42 using Intermediate 45 (300 mg, 1.218 mmol), PS-BEMP resin (1.108 g) and 4-methanesulfonyloxy-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 2) (374 mg, 1.34 mmol) in DMF (10 ml) to afford 265 mg (51%) of Intermediate 46 as a yellow oil. MS (M+1)=430.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423054B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-150fdb8a77df4999909115a7edd9ba62
출처 메모uspto-grants-2008_09