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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 412668생성일: 2026년 10월 24일

(S)-Benzyl piperidine-2-carboxylate → tert-butyl 2-[(2S)-2-[(benzyloxy)carbonyl]-1-piperidinyl]-1H-1,3-benzimidazole-1-carboxylate

https://huagongshe.com/ko/reaction/412668

반응식

참여 물질

역할이름HCID투입량
반응물(S)-Benzyl piperidine-2-carboxylateHCID 12436231—
반응물tert-Butyl 2-chloro-1H-benzo[d]imidazole-1-carboxylateHCID 23441223—
생성물tert-butyl 2-[(2S)-2-[(benzyloxy)carbonyl]-1-piperidinyl]-1H-1,3-benzimidazole-1-carboxylateHCID 59063194—

반응 단계

The title compound was prepared by a similar method to Preparation 2 from tert-butyl 2-chloro-1H-1,3-benzimidazole-1-carboxylate [see Preparation 46] and benzyl (2S)-2-piperidinecarboxylate [see J.A.C.S. (1 996), 118(7), 1629-1644]. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 90:10 changing to 80:20, by volume, hexane:ethyl acetate, in 5% increments to afford tert-butyl 2-[(2S)-2-[(benzyloxy)carbonyl]-1-piperidinyl]-1H-1,3-benzimidazole-1-carboxylate as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06562964B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-bae9e8ac8db7445da45c38f603f0c930
출처 메모uspto-grants-2003_05