Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-(N-tert-Butoxycarbonyl-N-methylamino)pyrrolidine → Hydrochloric Acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-(N-tert-Butoxycarbonyl-N-methylamino)pyrrolidine | HCID 2761404 | — |
| 반응물 | (S)-Methyl-pyrrolidin-3-yl-carbamic acid tert-butyl ester | HCID 7171888 | — |
| 반응물 | 4-Bromo-5-isoquinolinesulfonyl chloride | HCID 14580058 | — |
| 반응물 | 4-Chloroisoquinoline-5-sulfonyl chloride | HCID 22121908 | — |
| 생성물 | Hydrochloric Acid | HCID 313 | — |
| 생성물 | (S)-3-[N-(tert-butoxycarbonyl)-N-methylamino]-1-(4-chloro-5-isoquinolinesulfonyl)pyrrolidine | HCID 67243150 | — |
반응 단계
That is, (S)-3-[N-(tert-butoxycarbonyl)-N-methylamino]-1-(4-chloro-5-isoquinolinesulfonyl)pyrrolidine (Intermediate 21a) was prepared by using 4-chloro-5-isoquinolinesulfonyl chloride and (S)-3-[N-(tert-butoxycarbonyl)-N-methylamino]pyrrolidine in the method of Example 31, Step A instead of 4-bromo-5-isoquinolinesulfonyl chloride and 3-[N-(tert-butoxycarbonyl)-N-methylamino]pyrrolidine, respectively, and then used in the method of Example 31, Step B in a similar manner to obtain the compound of Example 19-3 as hydrochloride.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07618984B2 |
| 출처 데이터셋 | uspto-grants-2009_11 |
| ORD ID | ord-36cd2ec9352a481da8dd8a7ead237c0d |
| 출처 메모 | uspto-grants-2009_11 |