Water → 1-Amino-3-(difluoromethyl)-N-phenyl-1H-pyrrole-2-carboxamide

HRID 525022노트

반응식

HRID 525022 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

6

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

  1. customat room temperature
  2. customA thick suspension formed
  3. extractionextracted with ethyl acetate
  4. extractionThe aqueous layer was further extracted with ethyl acetate (2×)
  5. washThe combined organic layer was washed with water and brine
  6. dry with materialwas dried over sodium sulphate
  7. filtrationfiltered
  8. concentrationconcentrated
  9. 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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