3-[2-(4-Nitro-phenyl)-ethyl]-oxazolidin-2-one → 3-(2-(4-Aminophenyl)ethyl)-1,3-oxazolidin-2-one

HRID 1094015노트

반응식

HRID 1094015 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][N:12]2[CH2:16][CH2:15][O:14][C:13]2=[O:17])=[CH:6][CH:5]=1)([O-])=O.[H][H]>CO.[Pd]>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][N:12]2[CH2:16][CH2:15][O:14][C:13]2=[O:17])=[CH:6][CH:5]=1

참가 물질

5

반응물 2

HCID 107761683-[2-(4-Nitro-phenyl)-ethyl]-oxazolidin-2-oneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 107034763-(2-(4-Aminophenyl)ethyl)-1,3-oxazolidin-2-one

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

Pd/C 10% (500 mg) is added to a solution of the compound obtained in Step B (16.6 mmoles) in MeOH (100 ml). The reaction mixture is stirred at 50° C. under 4.5 bars of hydrogen for 4 hours. The catalyst is filtered off and then washed with MeOH. The filtrate is evaporated to dryness and the product obtained is triturated in 10 ml of MeOH. The solid obtained is filtered off and dried in vacuo at 40° C. overnight to yield the title product in the form of a white solid, which is used directly in the next Step.

후처리

  1. filtrationThe catalyst is filtered off
  2. washwashed with MeOH
  3. customThe filtrate is evaporated to dryness
  4. customthe product obtained
  5. customis triturated in 10 ml of MeOH
  6. customThe solid obtained
  7. filtrationis filtered off
  8. customdried in vacuo at 40° C. overnight

출처 및 근거

ORD 기록
ord-154339485dc2458b9a183fae320e5d75
출처 데이터셋
uspto-grants-2012_03
특허 번호
US08133889B2

반응 노트

불러오는 중…