(S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate → HCID 11265628, 화합물

HRID 1243810노트

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HRID 1243810 반응식
CON(C)[C:4](=[O:15])[C@@H:5]([NH:7][C:8](=[O:14])[O:9][C:10]([CH3:13])([CH3:12])[CH3:11])[CH3:6].[F:17][C:18]1[CH:23]=[CH:22][C:21]([Mg]Br)=[CH:20][CH:19]=1.O1CCCC1>O1CCCC1>[F:17][C:18]1[CH:23]=[CH:22][C:21]([C:4](=[O:15])[C@@H:5]([NH:7][C:8](=[O:14])[O:9][C:10]([CH3:11])([CH3:12])[CH3:13])[CH3:6])=[CH:20][CH:19]=1

참가 물질

4

실험 절차

A solution of t-butyl N-{(1S)-2-[methoxy(methyl)amino]-1-methyl-2-oxoethyl}carbamate (50 g) in tetrahydrofuran (700 mL) was gradually added dropwise at 0° C. to a 2.5M 4-fluorophenylmagnesium bromide/tetrahydrofuran solution (300 mL) which had been prepared previously. The mixture was stirred at room temperature for 14 hours, cooled to 0° C., and extracted twice with ether after addition of saturated aqueous sodium bicarbonate. The organic layer was washed successively with saturated aqueous sodium bicarbonate and saturated brine, and dried over anhydrous sodium sulfate. After removal of the sodium sulfate by filtration, the organic solvent was evaporated off in vacuo. The resulting residue was purified by column chromatography on silica gel (C-300; hexane:ethyl acetate=4:1) to give the title compound.

후처리

  1. customhad been prepared previously
  2. temperaturecooled to 0° C.
  3. extractionextracted twice with ether
  4. additionafter addition of saturated aqueous sodium bicarbonate
  5. washThe organic layer was washed successively with saturated aqueous sodium bicarbonate and saturated brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. customAfter removal of the sodium sulfate
  8. filtrationby filtration
  9. customthe organic solvent was evaporated off in vacuo
  10. customThe resulting residue was purified by column chromatography on silica gel (C-300; hexane:ethyl acetate=4:1)

출처 및 근거

ORD 기록
ord-9dc6862a05f64a3ea2958bc2d16a13b9
출처 데이터셋
uspto-grants-2006_10
특허 번호
US07119107B2

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