Dichloromethane → tert-butyl N-(4-cyano-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazol-2-yl)-beta-alaninate

HRID 17564노트

반응식

HRID 17564 반응식
Cl.[NH2:2][CH2:3][CH2:4][C:5]([O:7][C:8]([CH3:11])([CH3:10])[CH3:9])=[O:6].C(N(C(C)C)CC)(C)C.ClCCl.Cl[C:25]1[O:26][C:27]2[C:28](=[C:30]([C:42]#[N:43])[C:31]([CH3:41])=[C:32]([C:35]3[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=3)[C:33]=2[F:34])[N:29]=1>C(OCC)(=O)C>[C:42]([C:30]1[C:28]2[N:29]=[C:25]([NH:2][CH2:3][CH2:4][C:5]([O:7][C:8]([CH3:11])([CH3:10])[CH3:9])=[O:6])[O:26][C:27]=2[C:33]([F:34])=[C:32]([C:35]2[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=2)[C:31]=1[CH3:41])#[N:43]

참가 물질

6

실험 절차

With cooling with ice, tert-butyl 3-aminopropionate hydrochloride (230 mg, 1.26 mmol) and diisopropylethylamine (430 μl, 2.53 mmol) were added to a dichloromethane (10 ml) solution of 2-chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-cabonitrile (I-130) (302 mg, 1.05 mmol), followed by stirring at room temperature for 1 hour. The reaction liquid was cooled to room temperature, then ethyl acetate was added, and followed by washing with saturated brine. After drying over anhydrous sodium sulfate, the insoluble matter was separated by filtration, and the residue obtained by concentration was purified by silica gel column chromatography (eluent, n-hexane:ethyl acetate=4:1→1:1, v/v) to obtain the entitled compound (402 mg, 97%) as a white solid.

후처리

  1. customThe reaction liquid
  2. temperaturewas cooled to room temperature
  3. washby washing with saturated brine
  4. dry with materialAfter drying over anhydrous sodium sulfate
  5. customthe insoluble matter was separated by filtration
  6. customthe residue obtained by concentration
  7. customwas purified by silica gel column chromatography (eluent, n-hexane

출처 및 근거

ORD 기록
ord-4721cad7db674ea2bc7b4737ac727b8a
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07737166B2

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