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Water → 4-(2-Amino-1,3-thiazol-4-yl)benzonitrile

HRID 1436463
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HRID 1436463 반응식
[NH2:1][C:2]([NH2:4])=[S:3].[C:5]([C:7]1[CH:16]=[CH:15][C:10]([C:11](=O)[CH2:12]Br)=[CH:9][CH:8]=1)#[N:6].[OH-].[Na+].O>C(O)C>[NH2:1][C:2]1[S:3][CH:12]=[C:11]([C:10]2[CH:15]=[CH:16][C:7]([C:5]#[N:6])=[CH:8][CH:9]=2)[N:4]=1
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참가 물질

6

반응물 4

HCID 962WaterHCID 14798Sodium HydroxideHCID 986544-(Bromoacetyl)benzonitrileHCID 2723790Thiourea

생성물 1

HCID 20495894-(2-Amino-1,3-thiazol-4-yl)benzonitrile수율 90%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Thiourea (0.76 g, 10 mmol) was added to 4-cyanophenacyl bromide (2.0 g, 8.9 mmol) in ethanol (20 mL), and the reaction heated under reflux. After 45 min, the mixture was cooled to room temperature, and poured into 2N NaOH (10 mL)/water (40 mL). The precipitate was collected and air-dried to give 4-(2-amino-thiazol-4-yl)benzonitrile (1.6 g, 90%), which was used without further characterization.

후처리

  1. temperaturethe reaction heated
  2. temperatureunder reflux
  3. customThe precipitate was collected
  4. customair-dried

출처 및 근거

ORD 기록
ord-f829c169ee5646be8d2dcd12e1074985
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07618990B2

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