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2-Aminothiazole → HCID 13079789, 화합물

HRID 1284091
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HRID 1284091 반응식
Cl[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:7][CH:6]=1)=O.[NH2:17][C:18]1[S:19][CH:20]=[CH:21][N:22]=1>C(O)C>[S:19]1[CH:20]=[CH:21][N:22]2[CH:2]=[C:3]([C:5]3[CH:10]=[CH:9][C:8]([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:7][CH:6]=3)[N:17]=[C:18]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21552-AminothiazoleHCID 12399236HCID 12399236, 화합물

생성물 1

HCID 13079789HCID 13079789, 화합물수율 31%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 38 g of ethyl 4-(chloroacetyl)phenylacetate, 60 ml of ethanol and 32 g of 2-aminothiazole is heated under reflux for 2 hours. The ethanol is distilled off under reduced pressure, and water is added to the residue. The mixture is extracted with benzene, and the extract is washed with water, dried and concentrated. To the residual reddish brown oil are added benzene and isopropyl ether, and the crystalline precipitate is filtered off and recrystallized from ethanol to give 14 g of ethyl 4-(imidazo[2,1-b]-thiazol-6-yl)phenylacetate as colorless crystals melting at 117°-119°C.

후처리

  1. temperatureis heated
  2. temperatureunder reflux for 2 hours
  3. distillationThe ethanol is distilled off under reduced pressure, and water
  4. additionis added to the residue
  5. extractionThe mixture is extracted with benzene
  6. washthe extract is washed with water
  7. customdried
  8. concentrationconcentrated
  9. additionTo the residual reddish brown oil are added benzene and isopropyl ether
  10. filtrationthe crystalline precipitate is filtered off
  11. customrecrystallized from ethanol

출처 및 근거

ORD 기록
ord-e7e8f4f7c2bd44029754b4a61633afbf
출처 데이터셋
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03978071

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