Diisopropylamine → N,N-Dimethyl-2-(4-((trimethylsilyl)ethynyl)-1H-pyrazol-1-yl)acetamide

HRID 2205910노트

반응식

HRID 2205910 반응식
I[C:2]1[CH:3]=[N:4][N:5]([CH2:7][C:8]([N:10]([CH3:12])[CH3:11])=[O:9])[CH:6]=1.[CH3:13][Si:14]([C:17]#[CH:18])([CH3:16])[CH3:15].C(NC(C)C)(C)C.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>CN(C=O)C.[Cu]I.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH3:11][N:10]([CH3:12])[C:8](=[O:9])[CH2:7][N:5]1[CH:6]=[C:2]([C:18]#[C:17][Si:14]([CH3:16])([CH3:15])[CH3:13])[CH:3]=[N:4]1

참가 물질

8

반응 조건

온도
60 °C

실험 절차

2-(4-Iodo-1H-pyrazol-1-yl)-N,N-dimethylacetamide (Preparation 99, 0.68 g, 2.42 mmol) and trimethylsilylacetylene (0.326 g, 3.32 mmol) were dissolved in dry DMF (5 ml) and placed under argon. Diisopropylamine (0.47 ml, 3.3 mmol), copper (1) iodide (30 mg, 0.16 mmol), triphenylphosphine (126 mg, 0.242 mmol) and palladium acetate (40 mg, 0.16 mmol) were added and the flask was flushed with argon. The reaction was heated to 60° C. for 1 hour. The reaction was cooled to room temperature and diluted with ethyl acetate (30 ml). The organic solution was washed with water, brine, dried over sodium sulphate and filtered. The solvent was removed in vacuum and the crude purified on silica gel column chromatography eluting with neat ethyl acetate to afford the title compound as a pale yellow powder (0.55 g, 91%). 1H-NMR (500 MHz, CDCl3): δ 0.21 (s, 9H), 2.96 (s, 3H), 3.04 (s, 3H), 4.92 (s, 2H), 7.59 (s, 1H), 7.65 (s, 1H).

후처리

  1. customthe flask was flushed with argon
  2. temperatureThe reaction was cooled to room temperature
  3. additiondiluted with ethyl acetate (30 ml)
  4. washThe organic solution was washed with water, brine
  5. dry with materialdried over sodium sulphate
  6. filtrationfiltered
  7. customThe solvent was removed in vacuum
  8. customthe crude purified on silica gel column chromatography
  9. washeluting with neat ethyl acetate

출처 및 근거

ORD 기록
ord-c722d32839834f05a776eb7ceeaadf44
출처 데이터셋
uspto-grants-2016_06
특허 번호
US09371319B2

반응 노트

불러오는 중…