Methanamine, N-methoxy-, hydrochloride (1:1) → N-Methoxy-N-methyloxazole-4-carboxamide

HRID 1451347노트

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HRID 1451347 반응식
Cl.[CH3:2][O:3][NH:4][CH3:5].C[Al](C)C.[O:10]1[CH:14]=[C:13]([C:15]([O:17]C)=O)[N:12]=[CH:11]1.Cl.C(Cl)Cl>ClC(Cl)C>[O:10]1[CH:14]=[C:13]([C:15]([N:4]([CH3:5])[O:3][CH3:2])=[O:17])[N:12]=[CH:11]1

참가 물질

6

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온도
0 °C

실험 절차

To a suspension of methoxy-methylamine hydrochloride (2.3 g, 23.6 mmol) in 30 ml of dichloroethane at 0° C. was added dropwise 11.8 ml (23.6 mmol) of trimethylaluminum. The mixture was stirred at 0° C. for 20 min, methyl 4-oxazolecarboxylate (1 g, 7.9 mmol) in 20 ml of dichloroethane was added in one portion. The mixture was poured into an ice-cold solution of 0.5N HCl/methylene chloride (2:1) and stirred for 10 min. The aqueous layer was extracted with methylene chloride (2×50 ml), and the combined organic layer was washed with saturated ammonium chloride solution, dried over sodium sulfate, and concentrated in vacuo. The resulting residue was purified by chromatography on silica (methylene chloride/ethyl acetate/methanol 6:3:1) to afford 1.0 g (81.9%) of 4-oxazolyl-N-methyl-N-methoxy-carboxamide.

후처리

  1. stirringstirred for 10 min
  2. extractionThe aqueous layer was extracted with methylene chloride (2×50 ml)
  3. washthe combined organic layer was washed with saturated ammonium chloride solution
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe resulting residue was purified by chromatography on silica (methylene chloride/ethyl acetate/methanol 6:3:1)

출처 및 근거

ORD 기록
ord-f795f67b47f54a26927a38ca5cfd5a81
출처 데이터셋
uspto-grants-1997_02
특허 번호
US05604224

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