Triethylamine → HCID 59152162, 화합물

HRID 605590노트

반응식

HRID 605590 반응식
[C:1]([N:5]1[C:9]([NH:10][C:11]2[CH:16]=[N:15][CH:14]=[C:13](Cl)[N:12]=2)=[CH:8][CH:7]=[N:6]1)([CH3:4])([CH3:3])[CH3:2].[CH:18]([B-](F)(F)F)=[CH2:19].[K+].C(N(CC)CC)C>C(O)CC>[C:1]([N:5]1[C:9]([NH:10][C:11]2[CH:16]=[N:15][CH:14]=[C:13]([CH:18]=[CH2:19])[N:12]=2)=[CH:8][CH:7]=[N:6]1)([CH3:4])([CH3:3])[CH3:2]

참가 물질

5

반응 조건

온도
110 °C

실험 절차

A mixture of 65.04 g of N-(1-tert-butyl-1H-pyrazol-5-yl)-6-chloropyrazin-2-amine, 41.6 g of potassium vinyltrifluoroborate, 4.22 g of (1,1′-bis (diphenylphosphino)ferrocene)dichloropalladium(II) dichloromethane complex, 72 ml of triethylamine and 685 ml of 1-propanol was stirred at 110° C. overnight, followed by cooling down to room temperature and concentrated in vacuo. The obtained residue was diluted with ethyl acetate, and an insoluble matter was filtered off using Celite. The resulting ethyl acetate solution was washed with water, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo. The obtained residue was suspended in 100 ml of ethyl acetate, and 400 ml of diisopropylether was added to the mixture. The obtained precipitate was collected to give the title compound as a pale brown solid.

후처리

  1. temperatureby cooling down to room temperature
  2. concentrationconcentrated in vacuo
  3. additionThe obtained residue was diluted with ethyl acetate
  4. filtrationan insoluble matter was filtered off
  5. washThe resulting ethyl acetate solution was washed with water
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated in vacuo
  9. addition400 ml of diisopropylether was added to the mixture
  10. customThe obtained precipitate was collected

출처 및 근거

ORD 기록
ord-796fb5c675cc485293f5af6b0cf0d8dd
출처 데이터셋
uspto-grants-2011_03
특허 번호
US07915263B2

반응 노트

불러오는 중…