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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1745466생성일: 2026년 10월 26일

Tert-butyl 4-(trifluoromethanesulfonyloxy)-1,2,3,6-tetrahydropyridine-1-carboxylate → 4-(4-tert.-Butoxycarbonylamino-3-nitro-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert.-butyl ester

https://huagongshe.com/reaction/1745466

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butyl 4-(trifluoromethanesulfonyloxy)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 10991161—
반응물(2-Nitro-4-tributylstannanyl-phenyl)-carbamic acid tert.-butyl esterHCID 23554337—
생성물4-(4-tert.-Butoxycarbonylamino-3-nitro-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert.-butyl esterHCID 6959283752%

반응 단계

Prepared from (2-nitro-4-tributylstannanyl-phenyl)-carbamic acid tert.-butyl ester (Example D2) (3.18 g, 6.06 mmol) and 4-trifluoromethylsulfonyloxy-3,6-dihydro-2H-pyridine-1-carboxylic acid tert.-butyl ester (1.99 g, 6.0 mmol) [prepared from Boc-4-piperidone by treatment with LDA in THF at −78° C. followed by reaction with N-phenyl-bis(trifluoromethanesulfonimide) according to Wustrow et al. Synthesis 1991, 1993] according to the general procedure E. Obtained as an orange solid (1.304 g, 52%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07018998B2
출처 데이터셋uspto-grants-2006_03
ORD IDord-03654413fdb94f3da639e8ca0dfaab03
출처 메모uspto-grants-2006_03