Ammonia → 3-Chloro-4-(4-phenylpyrimidin-2-ylamino)benzamide

HRID 1473856노트

반응식

HRID 1473856 반응식
C[Al](C)C.[NH3:5].O1CCOCC1.[Cl:12][C:13]1[CH:14]=[C:15]([CH:19]=[CH:20][C:21]=1[NH:22][C:23]1[N:28]=[C:27]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH:26]=[CH:25][N:24]=1)[C:16]([O-])=[O:17]>C(Cl)Cl>[Cl:12][C:13]1[CH:14]=[C:15]([CH:19]=[CH:20][C:21]=1[NH:22][C:23]1[N:28]=[C:27]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH:26]=[CH:25][N:24]=1)[C:16]([NH2:5])=[O:17]

참가 물질

6

반응물 4

HCID 222AmmoniaHCID 312751,4-DioxaneHCID 16682925TrimethylaluminumHCID 866478723-Chloro-4-(4-phenylpyrimidin-2-ylamino)benzoate

생성물 1

HCID 595881623-Chloro-4-(4-phenylpyrimidin-2-ylamino)benzamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Trimethylaluminum (0.8 mL, 2.0 mmol, 2.5M in hexanes) was slowly added to a solution of ammonia in dioxane (4 mL, 0.5 mmol) under argon at room temperature. After stirring for 15 min at room temperature, 3-chloro-4-(4-phenylpyrimidin-2-ylamino)benzoate (0.67 g, 2.0 mmol) in CH2Cl2 was added slowly. The mixture was stirred at room temperature until the ester had been consumed as judged by analytical HPLC analysis. The reaction was quenched with 1 N HCl and the layers were separated. The aqueous layer was extracted with CH2Cl2 (2×), and the combined organics were dried (MgSO4) and concentrated to afford (3-chloro-4-(4 phenylpyrimidin-2-ylamino)benzamide. MS (ESI) 325 (M+H).

후처리

  1. customhad been consumed
  2. customThe reaction was quenched with 1 N HCl
  3. customthe layers were separated
  4. extractionThe aqueous layer was extracted with CH2Cl2 (2×)
  5. dry with materialthe combined organics were dried (MgSO4)
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-1f70c260b8ee460ca0d190868f5d6053
출처 데이터셋
uspto-grants-2015_04
특허 번호
US09018205B2

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