Potassium Carbonate → 2-(2,5-Dichloro-pyrimidin-4-ylamino)-5-morpholin-4-yl-benzamide

HRID 1040843노트

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HRID 1040843 반응식
[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([N:11]2[CH2:16][CH2:15][O:14][CH2:13][CH2:12]2)=[CH:7][C:3]=1[C:4]([NH2:6])=[O:5].[Cl:17][C:18]1[N:23]=[C:22](Cl)[C:21]([Cl:25])=[CH:20][N:19]=1.C(=O)([O-])[O-].[K+].[K+]>C1COCC1.O>[Cl:17][C:18]1[N:23]=[C:22]([NH:1][C:2]2[CH:10]=[CH:9][C:8]([N:11]3[CH2:12][CH2:13][O:14][CH2:15][CH2:16]3)=[CH:7][C:3]=2[C:4]([NH2:6])=[O:5])[C:21]([Cl:25])=[CH:20][N:19]=1

참가 물질

6

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온도
50 °C

실험 절차

A mixture of 2-amino-5-morpholin-4-yl-benzamide (820.0 mg, 3.71 mmol, Heterocyclic Comm. 2001, 7, 473-480), 2,4,5-trichloropyrimidine (679.8 mg, 3.71 mmol) and potassium carbonate (614.6 mg, 4.45 mol) in THF (10 mL) was stirred at 50° C. for 20 h and at RT for 6 days. The reaction was diluted with water (10 mL) and extracted into EtOAc. The organic layer was washed with NaHCO3, brine and dried by passing through a funnel filled with MgSO4. The filtrate was evaporated and the residue triturated with ether (5×3 mL) to afford 2-(2,5-dichloro-pyrimidin-4-ylamino)-5-morpholin-4-yl-benzamide as a yellow solid (0.75 g) that was used without further purification in the subsequent step.

후처리

  1. extractionextracted into EtOAc
  2. washThe organic layer was washed with NaHCO3, brine
  3. customdried
  4. customby passing through a funnel
  5. additionfilled with MgSO4
  6. customThe filtrate was evaporated
  7. customthe residue triturated with ether (5×3 mL)

출처 및 근거

ORD 기록
ord-091c4b06504d44988d6c533b66c058a0
출처 데이터셋
uspto-grants-2013_10
특허 번호
US08552186B2

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