Ammonia → Diammonium[(6-bromo-2-cyanoquinolin-7-yl)(difluoro)methyl]phosphonate

HRID 1422585노트

반응식

HRID 1422585 반응식
C([O:3][P:4]([C:9]([C:12]1[CH:21]=[C:20]2[C:15]([CH:16]=[CH:17][C:18]([C:22]#[N:23])=[N:19]2)=[CH:14][C:13]=1[Br:24])([F:11])[F:10])(=[O:8])[O:5]CC)C.Br[Si](C)(C)C.[NH3:30].CO>ClCCl>[Br:24][C:13]1[CH:14]=[C:15]2[C:20](=[CH:21][C:12]=1[C:9]([P:4](=[O:3])([O-:5])[O-:8])([F:11])[F:10])[N:19]=[C:18]([C:22]#[N:23])[CH:17]=[CH:16]2.[NH4+:30].[NH4+:19]

참가 물질

6

실험 절차

To a stirred solution of diethyl[(6-bromo-2-cyanoquinolin-7-yl)(difluoro)methyl]phosphonate (370 mg, 0.883 mmol) in dichloromethane (9) at 0° C. was added dropwise bromotrimethylsilane (1.15 mL, 8.83 mmol). The reaction mixture was stirred at room temperature overnight. It was concentrated to dryness, and co-evaporated with dichloromethane (2×). Ethanol (5 mL) was added to the residue, which was stirred for 20 minutes. It was concentrated to dryness and co-evaporated with ethanol (2×). The residue was dissolved in methanol (8 mL) and 2.0 M ammonia in methanol (4.4 mL, 8.80 mmol) was added dropwise. It was stirred for 20 minutes, concentrated to dryness and suspended in diethyl ether. The precipitate was filtered to afford diammonium[(6-bromo-2-cyanoquinolin-7-yl)(difluoro)methyl]phosphonate.

후처리

  1. concentrationIt was concentrated to dryness
  2. additionEthanol (5 mL) was added to the residue, which
  3. stirringwas stirred for 20 minutes
  4. concentrationIt was concentrated to dryness and co-evaporated with ethanol (2×)
  5. dissolutionThe residue was dissolved in methanol (8 mL)
  6. stirringIt was stirred for 20 minutes
  7. concentrationconcentrated to dryness
  8. filtrationThe precipitate was filtered

출처 및 근거

ORD 기록
ord-1cdb1480de7043a7a49e14a8cc2f6609
출처 데이터셋
uspto-grants-2015_01
특허 번호
US08927526B2

반응 노트

불러오는 중…