Chloride → methyl 3-{4-[2-(acetylmethylamino)thiazol-5-yl]phenyl}-2(S)-ethoxypropanoate

HRID 2426308노트

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HRID 2426308 반응식
[Cl-].Br[C:3]1[S:7][C:6]([N:8](C)[C:9](=O)C)=[N:5][CH:4]=1.[CH2:13]([O:15][C@@H:16]([CH2:21][C:22]1[CH:27]=[CH:26][C:25](B2OC(C)(C)C(C)(C)O2)=[CH:24][CH:23]=1)[C:17]([O:19][CH3:20])=[O:18])[CH3:14].[F-].[Cs+].CO[CH2:41][CH2:42][O:43]C>>[C:42]([CH2:9][NH:8][C:6]1[S:7][C:3]([C:25]2[CH:24]=[CH:23][C:22]([CH2:21][C@H:16]([O:15][CH2:13][CH3:14])[C:17]([O:19][CH3:20])=[O:18])=[CH:27][CH:26]=2)=[CH:4][N:5]=1)(=[O:43])[CH3:41]

참가 물질

6

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온도
80 °C

실험 절차

0.2 g (0.3 mmol) of diphenylphosphinoferrocenepalladium chloride (PdCl2dppf) is added to a solution of 1 g (4.5 mmol) of N-(5-bromothiazol-2-yl)-N-methylacetamide, 1.8 g (6.8 mmol) of methyl 2(S)-ethoxy-3-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl]propanoate and 1 g (6.8 mmol) of caesium fluoride in 50 ml of ethylene glycol dimethyl ether, degassed beforehand. The reaction medium is heated at 80° C. for 18 hours. After cooling, water is added and the reaction medium is extracted with ethyl acetate. The ethyl acetate phase is washed with saturated sodium chloride solution, dried over magnesium sulfate, filtered and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with a 70/30 and then 60/40 heptane/ethyl acetate mixture. 0.6 g (37%) of methyl 3-{4-[2-(acetylmethylamino)thiazol-5-yl]phenyl}-2(S)-ethoxypropanoate is obtained in the form of a beige-colored solid with a melting point of 123° C.

후처리

  1. customdegassed beforehand
  2. temperatureAfter cooling
  3. additionwater is added
  4. extractionthe reaction medium is extracted with ethyl acetate
  5. washThe ethyl acetate phase is washed with saturated sodium chloride solution
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. customevaporated
  9. customThe residue obtained
  10. customis purified by chromatography on a column of silica
  11. washeluted with a 70/30

출처 및 근거

ORD 기록
ord-33f4ef09b01f40619de3308048ba19d6
출처 데이터셋
uspto-grants-2011_06
특허 번호
US07968560B2

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