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HRID 1962439생성일: 2026년 10월 24일

tert-butyl N-[(3S)-piperidin-3-yl]carbamate → Hydrochloric Acid

https://huagongshe.com/ko/reaction/1962439

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl N-[(3S)-piperidin-3-yl]carbamateHCID 1514171—
반응물4-Chloroisoquinoline-5-sulfonyl chlorideHCID 22121908—
생성물Hydrochloric AcidHCID 3131,932.7%
생성물(S)-3-(tert-Butoxycarbonylamino)-1-(4-chloro-5-isoquinolinesulfonyl)piperidineHCID 67243279—
생성물(S)-3-Amino-1-(4-chloro-5-isoquinolinesulfonyl)piperidineHCID 67244043—

반응 단계

(S)-3-(tert-Butoxycarbonylamino)-1-(4-chloro-5-isoquinolinesulfonyl)-piperidine (Intermediate 18a) was prepared from 4-chloro-5-isoquinolinesulfonyl chloride (183 mg) and (S)-3-(tert-butoxycarbonylamino)piperidine (168 mg) according to the method described in Example 1-1, Step A, and then used in the method of Example 1-1, Step B in a similar manner to obtain the title compound as hydrochloride (164 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08415372B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-66e2bd0e5d04453c84eade2bb4c82cdb
출처 메모uspto-grants-2013_04