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

HCID 18738443, 화합물 → HCID 18738434, 화합물

HRID 1934468
노트
인쇄 미리보기

반응식

HRID 1934468 반응식
[N:1]1([S:7]([CH2:10][C@H:11]([CH3:22])[C:12]([O:14]CC2C=CC=CC=2)=[O:13])(=[O:9])=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1>[Pd]>[N:1]1([S:7]([CH2:10][C@H:11]([CH3:22])[C:12]([OH:14])=[O:13])(=[O:9])=[O:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 18738443HCID 18738443, 화합물

생성물 1

HCID 18738434HCID 18738434, 화합물

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

A 100 mL Fisher/Porter vessel was charged with 1 g of benzyl 3-(1-piperidinyl)sulfonyl-2(R)-methylpropionate 30 mL MeOH and a catalytic amount of 10% Pd—C. The reaction was hydrogenated at 50 psi for 3 hours. After filtration through Celite and concentration in vacuo of 3-(1-piperidinyl)sulfonyl-2(R)-methylpropionic acid was isolated in quantitive yield.

후처리

  1. filtrationAfter filtration
  2. concentrationthrough Celite and concentration in vacuo of 3-(1-piperidinyl)sulfonyl-2(R)-methylpropionic acid
  3. customwas isolated in quantitive yield

출처 및 근거

ORD 기록
ord-dcef4994de94407c8aed218d4fcaf97a
출처 데이터셋
uspto-grants-2002_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06384036B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트