Water → 1-Amino-3-(difluoromethyl)-N-phenyl-1H-pyrrole-2-carboxamide
반응식
C[Si]([N-][Si](C)(C)C)(C)C.[Li+].[F:11][CH:12]([F:27])[C:13]1[CH:17]=[CH:16][NH:15][C:14]=1[C:18]([NH:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[O:19].C1(P(C2C=CC=CC=2)(=O)[NH2:35])C=CC=CC=1.O>CN(C=O)C>[NH2:35][N:15]1[CH:16]=[CH:17][C:13]([CH:12]([F:11])[F:27])=[C:14]1[C:18]([NH:20][C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)=[O:19]참가 물질
실험 절차
1.1 ml (1.1 mmol) of a 1M solution of lithium bis(trimethylsilyl)amide was added to a solution of 3-(difluoromethyl)-N-phenyl-1H-pyrrole-2-carboxamide (100 mg, 0.42 mmol) and DPPONH2 (P,P-diphenylphosphinic amide, available from Sigma Aldrich®, cat. no. 5994-87-6) (250 mg, 1,1 mmol) in DMF (4 mL) at room temperature. A thick suspension formed and additional 4 mL of DMF were added. The mixture was stirred at room temperature for 1 hour and then it was poured into 50 mL of water and extracted with ethyl acetate. The aqueous layer was further extracted with ethyl acetate (2×). The combined organic layer was washed with water and brine and was dried over sodium sulphate, filtered and concentrated. The crude product was purified by flash chromatography (0% to 33% AcOEt/Hexanes) to yield 40 mg (38% yield) of the title compound.
후처리
- customat room temperature
- customA thick suspension formed
- extractionextracted with ethyl acetate
- extractionThe aqueous layer was further extracted with ethyl acetate (2×)
- washThe combined organic layer was washed with water and brine
- dry with materialwas dried over sodium sulphate
- filtrationfiltered
- concentrationconcentrated
- customThe crude product was purified by flash chromatography (0% to 33% AcOEt/Hexanes)
출처 및 근거
- ORD 기록
- ord-41ba3a249a234264a3f78ed7a26965f2
- 출처 데이터셋
- uspto-grants-2016_05
- 특허 번호
- US09340547B2
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