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1,1'-Carbonyldiimidazole → HCID 59323900, 화합물

HRID 2355045
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HRID 2355045 반응식
[NH2:1][C:2]1[S:3][C:4]([C:8]2[CH:13]=[CH:12][C:11]([C:14](=[O:16])[CH3:15])=[CH:10][CH:9]=2)=[C:5]([CH3:7])[N:6]=1.[C:17](N1C=CN=C1)([N:19]1[CH:23]=[CH:22][N:21]=[CH:20]1)=[O:18]>C1COCC1.ClCCl>[C:14]([C:11]1[CH:12]=[CH:13][C:8]([C:4]2[S:3][C:2]([NH:1][C:17]([N:19]3[CH:23]=[CH:22][N:21]=[CH:20]3)=[O:18])=[N:6][C:5]=2[CH3:7])=[CH:9][CH:10]=1)(=[O:16])[CH3:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 682631,1'-CarbonyldiimidazoleHCID 59383111HCID 59383111, 화합물

생성물 1

HCID 59323900HCID 59323900, 화합물

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 8028Tetrahydrofuran용매

반응 조건

온도
50 °C

실험 절차

A solution of 1-[4-(2-Amino-4-methyl-thiazol-5-yl)-phenyl]-ethanone (0.57 g, 2.45 mmol) is dissolved in a mixture of THF (10 ml) and dichloromethane (20 ml) and heated in an oil bath set to 50° C. Carbonyldiimidazole is added (0.64 g, 3.92 mmol) and the reaction mixture heated at 50° C. for a further 2 hours in which a pale yellow precipitate forms. After cooling to room temperature the precipitate is filtered, washed with dichloromethane and dried under high vacuum.

후처리

  1. temperatureheated in an oil bath
  2. customset to 50° C
  3. temperatureAfter cooling to room temperature the precipitate
  4. filtrationis filtered
  5. washwashed with dichloromethane
  6. customdried under high vacuum

출처 및 근거

ORD 기록
ord-fe7244ff477f4c2daca2389e32a66433
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07754746B2

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