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

HRID 1191069
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HRID 1191069 반응식
[C:1]([C:3]1[CH:12]=[CH:11][C:6]([C:7](=O)[CH2:8]Br)=[CH:5][CH:4]=1)#[N:2].[NH2:13][C:14]([NH2:16])=[S:15].C(=O)(O)[O-].[Na+]>C(O)C>[NH2:16][C:14]1[S:15][CH:8]=[C:7]([C:6]2[CH:11]=[CH:12][C:3]([C:1]#[N:2])=[CH:4][CH:5]=2)[N:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 986544-(Bromoacetyl)benzonitrileHCID 516892Sodium BicarbonateHCID 2723790Thiourea

생성물 1

HCID 20495894-(2-Amino-1,3-thiazol-4-yl)benzonitrile

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Slurry 4-cyanophenacyl bromide (40 g, 179 mmol), thiourea (13.6 g, 181 mmol) and sodium bicarbonate (15.3 g, 181 mmol) in absolute ethanol (560 mL). Stir the mixture at reflux for 20 h under a nitrogen atmosphere. Cool the slurry to room temperature, filter, wash the solids with ethanol (100 mL), water (3×75 mL) and hexane (3×75 mL). Collect the yellow solid, add water (200 mL) and stir the slurry for 30 min at room temperate. Filter and wash the solid with hexane (excess). Slurry the solid in EtOAc (50 mL) and concentrate in vacuo twice to remove residual water. Collect the desired intermediate as a light yellow solid (36 g, 99%). MS (ES+) m/z: 202.1 (M+H)+.

후처리

  1. temperatureat reflux for 20 h under a nitrogen atmosphere
  2. filtrationfilter
  3. washwash the solids with ethanol (100 mL), water (3×75 mL) and hexane (3×75 mL)
  4. customCollect the yellow solid
  5. additionadd water (200 mL)
  6. stirringstir the slurry for 30 min at room temperate
  7. filtrationFilter
  8. washwash the solid with hexane (excess)
  9. concentrationconcentrate in vacuo twice
  10. customto remove residual water
  11. customCollect the desired intermediate as a light yellow solid (36 g, 99%)

출처 및 근거

ORD 기록
ord-06f2fc3fe8a7410d849a4c8fe73f0ea8
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08680091B2

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