홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

tert-Butyl 3-amino-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate → 1,4,5,6-Tetrahydropyrrolo[3,4-c]pyrazol-3-amine

HRID 241565
노트
인쇄 미리보기

반응식

HRID 241565 반응식
[NH2:1][C:2]1[C:3]2[CH2:9][N:8](C(OC(C)(C)C)=O)[CH2:7][C:4]=2[NH:5][N:6]=1.C(O)(C(F)(F)F)=O.C(Cl)Cl>>[NH:5]1[C:4]2[CH2:7][NH:8][CH2:9][C:3]=2[C:2]([NH2:1])=[N:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 11333571tert-Butyl 3-amino-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylateHCID 21863450Trifluoroacetic acid methylene chloride

생성물 1

HCID 167845751,4,5,6-Tetrahydropyrrolo[3,4-c]pyrazol-3-amine

실험 절차

tert-Butyl 3-amino-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate (3670 mg, 16.36 mmol) was treated with TFA/CH2Cl2 (v/v=1/1) for 1 h. The reaction mixture was concentrated and the residue was treated with CH2Cl2/hexanes and then concentrated to give a solid. The product was passed through ion-exchange resin Strata X—C™ to give the title product (LC-MS: 125.05 (M+1)

후처리

  1. concentrationThe reaction mixture was concentrated
  2. additionthe residue was treated with CH2Cl2/hexanes
  3. concentrationconcentrated
  4. customto give a solid

출처 및 근거

ORD 기록
ord-9e6bd68a5bcb4f4c9408edfaa97042ae
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08653059B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트