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HRID 1436048생성일: 2026년 10월 25일

3-(N-tert-Butoxycarbonyl-N-methylamino)pyrrolidine → Hydrochloric Acid

https://huagongshe.com/reaction/1436048

반응식

참여 물질

역할이름HCID투입량
반응물3-(N-tert-Butoxycarbonyl-N-methylamino)pyrrolidineHCID 2761404—
반응물tert-Butyl methyl((3R)-pyrrolidin-3-yl)carbamateHCID 7019173—
반응물5-Isoquinolinesulfonyl chloride,4-bromo-1-chloro-HCID 76851490—
반응물1-Chloro-4-fluoro-5-isoquinolinesulfonyl chlorideHCID 86613861—
생성물Hydrochloric AcidHCID 313—
생성물(R)-3-[N-(tert-Butoxycarbonyl)-N-methylamino]-1-(1-chloro-4-fluoro-5-isoquinolinesulfonyl)pyrrolidineHCID 86613860—
생성물HCID 178484870HCID 178484870—

반응 단계

(R)-3-[N-(tert-Butoxycarbonyl)-N-methylamino]-1-(1-chloro-4-fluoro-5-isoquinolinesulfonyl)pyrrolidine (Intermediate 27b) is prepared by using 1-chloro-4-fluoro-5-isoquinolinesulfonyl chloride and (R)-3-[N-(tert-butoxy-carbonyl)-N-methylamino]pyrrolidine in the method of Example 35, Step A instead of 1-chloro-4-bromo-5-isoquinolinesulfonyl chloride and 3-[N-(tert-butoxycarbonyl)-N-methylamino]pyrrolidine, respectively, and then used in the method of Example 35, Step B in a similar manner to obtain the title compound as hydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07618984B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-5898350fbe1642688eb02f66d9a5eb81
출처 메모uspto-grants-2009_11