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

Hydrazine hydrate (1:1) → HCID 11075364, 화합물

HRID 1003700
노트
인쇄 미리보기

반응식

HRID 1003700 반응식
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH2:7][CH2:8][N:9]([CH2:13][CH2:14][CH2:15][CH2:16][N:17]3C(=O)C4=CC=CC=C4C3=O)[CH2:10]2)=[CH:5][CH:4]=1.O.NN>C(O)C>[NH2:17][CH2:16][CH2:15][CH2:14][CH2:13][N:9]1[CH2:8][CH2:7][C:6]2[C:11](=[CH:12][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)[CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 221325287-Methoxy-2-(4-phthalimidobutyl)-1,2,3,4-tetrahydroisoquinoline

생성물 1

HCID 11075364HCID 11075364, 화합물수율 63%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 7-methoxy-2-(4-phthalimidobutyl)-1,2,3,4-tetrahydroisoquinoline (17.4 g 0.0478 mol) and hydrazine monohydrate (4.6 ml, 0.095 mol) in ethanol (300 ml) were stirred at room temperature for 18 h and at reflux for 1 h. The cooled reaction mixture was filtered and the filtrate evaporated in vacuo. The residue was dissolved in 2.5N hydrochloric acid, filtered through Kieselguhr and the filtrate basified with 0.880 ammonia. The product was extracted into dichloromethanc (4×200 ml), the combined extracts were dried (Na2SO4) and evaporated in vacuo to afford the title compound as a brown oil (7 g, 63%).

후처리

  1. temperatureat reflux for 1 h
  2. customThe cooled reaction mixture
  3. filtrationwas filtered
  4. customthe filtrate evaporated in vacuo
  5. dissolutionThe residue was dissolved in 2.5N hydrochloric acid
  6. filtrationfiltered through Kieselguhr
  7. extractionThe product was extracted into dichloromethanc (4×200 ml)
  8. dry with materialthe combined extracts were dried (Na2SO4)
  9. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-098c271a09bf4d6ca5e79275ec5c86c5
출처 데이터셋
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06046210

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트