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

2-Benzyl-1-(1-pyrrolidinylmethyl)-1,2,3,4-tetrahydroisoquinoline → 1-(Pyrrolidin-1-ylmethyl)-1,2,3,4-tetrahydroisoquinoline

HRID 1382233
노트
인쇄 미리보기

반응식

HRID 1382233 반응식
C([N:8]1[CH2:17][CH2:16][C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]1[CH2:18][N:19]1[CH2:23][CH2:22][CH2:21][CH2:20]1)C1C=CC=CC=1>C(O)C.[Pd]>[N:19]1([CH2:18][CH:9]2[C:10]3[C:15](=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH2:16][CH2:17][NH:8]2)[CH2:23][CH2:22][CH2:21][CH2:20]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 212745372-Benzyl-1-(1-pyrrolidinylmethyl)-1,2,3,4-tetrahydroisoquinoline

생성물 1

HCID 147260101-(Pyrrolidin-1-ylmethyl)-1,2,3,4-tetrahydroisoquinoline수율 97.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

8 g of 2-benzyl-1-(1-pyrrolidinylmethyl)-1,2,3,4-tetrahydroisoquinoline were dissolved in 200 ml of 95% ethanol and hydrogenated on 1.5 g of 5% Pd on charcoal at 40° C. and room temperature. After 7 hr the catalyst was filtered off, and the solvent evaporated i.v. 5.5 g of crude product were obtained, sufficiently pure for the subsequent step.

후처리

  1. filtrationAfter 7 hr the catalyst was filtered off
  2. customthe solvent evaporated i.v

출처 및 근거

ORD 기록
ord-3f80a31861a04eb2a0894854f512516f
출처 데이터셋
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04806547

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트