Sodium Cyanide → 4-cyano-2,5-difluoro-N-[2,6-dimethyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenyl]-3-nitro-benzamide

HRID 1943120노트

반응식

HRID 1943120 반응식
[CH3:1][C:2]1[CH:7]=[C:6]([C:8]([F:17])([C:13]([F:16])([F:15])[F:14])[C:9]([F:12])([F:11])[F:10])[CH:5]=[C:4]([CH3:18])[C:3]=1[NH:19][C:20](=[O:33])[C:21]1[CH:26]=[C:25]([F:27])[C:24](F)=[C:23]([N+:29]([O-:31])=[O:30])[C:22]=1[F:32].[C-:34]#[N:35].[Na+]>CN(C)C=O>[C:34]([C:24]1[C:25]([F:27])=[CH:26][C:21]([C:20]([NH:19][C:3]2[C:2]([CH3:1])=[CH:7][C:6]([C:8]([F:17])([C:13]([F:15])([F:16])[F:14])[C:9]([F:12])([F:11])[F:10])=[CH:5][C:4]=2[CH3:18])=[O:33])=[C:22]([F:32])[C:23]=1[N+:29]([O-:31])=[O:30])#[N:35]

참가 물질

4

반응 조건

온도
0 °C

실험 절차

To a solution of N-[2,6-dimethyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenyl]-3-nitro-2,4,5-trifluoro-benzamide (6.77 g, 13.75 mmol) (Example I15) in N,N-dimethylformamide (137 ml) at 0° C. was added sodium cyanide (740 mg, 15.13 mmol). The reaction mixture was stirred at 0° C. for one hour and then at ambient temperature for 16 hours. The reaction mixture was concentrated and the residue partitioned between water and dichloromethane. The combined organic phases were dried over sodium sulfate and concentrated. The residue was purified by column chromatography on silica gel (eluent: cyclohexane/ethyl acetate 8:2) to give 4-cyano-2,5-difluoro-N-[2,6-dimethyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenyl]-3-nitro-benzamide (3.2 g, 46.6% yield). 1H-NMR (400 MHz, CDCl3): 2.35 (6H, s), 7.38 (2H, s), 7.83 (1H, d), 8.29 (1H, m) ppm.

후처리

  1. customat 0° C.
  2. waitat ambient temperature for 16 hours
  3. concentrationThe reaction mixture was concentrated
  4. customthe residue partitioned between water and dichloromethane
  5. dry with materialThe combined organic phases were dried over sodium sulfate
  6. concentrationconcentrated
  7. customThe residue was purified by column chromatography on silica gel (eluent: cyclohexane/ethyl acetate 8:2)

출처 및 근거

ORD 기록
ord-9c8eb3061c26414ebc0e338972844bcb
출처 데이터셋
uspto-grants-2013_03
특허 번호
US08389766B2

반응 노트

불러오는 중…