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Thionyl Chloride → 4-Chloro-5-ethyl-1H-imidazole-2-carbonyl chloride

HRID 43561
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HRID 43561 반응식
S(Cl)([Cl:3])=O.[Cl:5][C:6]1[N:7]=[C:8]([C:13]([OH:15])=O)[NH:9][C:10]=1[CH2:11][CH3:12]>>[Cl:5][C:6]1[N:7]=[C:8]([C:13]([Cl:3])=[O:15])[NH:9][C:10]=1[CH2:11][CH3:12]
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참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 675489294-chloro-5-ethyl-1H-imidazole-2-carboxylic acid

생성물 1

HCID 866485554-Chloro-5-ethyl-1H-imidazole-2-carbonyl chloride

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온도
85 °C

실험 절차

Thionyl chloride (4 mL) was added to 4-chloro-5-ethyl-1H-imidazole-2-carboxylic acid (described in Example 1c, 200 mg, 0.8 mmol), and the mixture was stirred at 85° C. for 40 minutes. Following concentration under reduced pressure, the residue was azeotropically distilled with toluene twice to obtain crude 4-chloro-5-ethyl-1H-imidazole-2-carboxylic acid chloride. 5 mL pyridine was added and then ethyl 2-(4-aminophenyl)-1,3-thiazole-5-carboxylate obtained in Example (91b) was added. The mixture was stirred at room temperature for one hour. The reaction solution was diluted with ethyl acetate. The precipitated solid was collected by filtration and washed with ethyl acetate, to obtain 214 mg of the title compound as a white solid (73%).

후처리

  1. concentrationconcentration under reduced pressure
  2. distillationthe residue was azeotropically distilled with toluene twice

출처 및 근거

ORD 기록
ord-7363586aa9954a2bae59faa273ee7a24
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08536197B2

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