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HCID 10447619, 화합물 → 2-(1H-Imidazol-1-yl)-1-{2-[(2-methoxyphenoxy)methyl]-1,3-thiazolidin-3-yl}ethan-1-one

HRID 2291916
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HRID 2291916 반응식
[NH:1]1[CH:5]=[CH:4][N:3]=[C:2]1[Na].Cl[CH2:8][C:9]([N:11]1[CH2:15][CH2:14][S:13][CH:12]1[CH2:16][O:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[O:24][CH3:25])=[O:10]>CS(C)=O>[N:1]1([CH2:8][C:9]([N:11]2[CH2:15][CH2:14][S:13][CH:12]2[CH2:16][O:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=2[O:24][CH3:25])=[O:10])[CH:5]=[CH:4][N:3]=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10447619HCID 10447619, 화합물HCID 178507081HCID 178507081, 화합물

생성물 1

HCID 30254562-(1H-Imidazol-1-yl)-1-{2-[(2-methoxyphenoxy)methyl]-1,3-thiazolidin-3-yl}ethan-1-one수율 79.6%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

Imidazolyl sodium (3.58 g) is added to a stirred solution of 3-chloroacetyl-2-(o-methoxyphenoxy)methylthiazolidine (5.8 g) in DMSO (35 ml). After 1 hour the mixture is poured in ice and water (200 ml) and the separated oil is extracted with EtOAc (3×30). The organic phases are collected, washed with water, dried on Na2SO4. After evaporation, the crude residue is purified by filtration on a short column of SiO2 using EtOAc and EtOAc/MeOH 85:15 as the eluent to give 3-(imidazol-1-yl)acetyl-2-(o-methoxyphenoxy)methyl-thiazolidine (5.1 g) as a colourless oil.

후처리

  1. additionAfter 1 hour the mixture is poured in ice
  2. extractionwater (200 ml) and the separated oil is extracted with EtOAc (3×30)
  3. customThe organic phases are collected
  4. washwashed with water
  5. customdried on Na2SO4
  6. customAfter evaporation
  7. filtrationthe crude residue is purified by filtration on a short column of SiO2

출처 및 근거

ORD 기록
ord-e45f96d681134d22b0dac77ac75044d0
출처 데이터셋
uspto-grants-1989_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04798898

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