Dimethylformamide dimethyl acetal → 3-(Dimethylaminomethyleneamino)benzofuran-2-carboxylic Acid Ethyl Ester

HRID 2213770

반응식

HRID 2213770 반응식
[NH2:1][C:2]1[C:3]2[CH:15]=[CH:14][CH:13]=[CH:12][C:4]=2[O:5][C:6]=1[C:7]([O:9][CH2:10][CH3:11])=[O:8].CO[CH:18](OC)[N:19]([CH3:21])[CH3:20]>>[CH2:10]([O:9][C:7]([C:6]1[O:5][C:4]2[CH:12]=[CH:13][CH:14]=[CH:15][C:3]=2[C:2]=1[N:1]=[CH:18][N:19]([CH3:21])[CH3:20])=[O:8])[CH3:11]

참가 물질

3

실험 절차

A mixture of 4.2 g (20.0 mmol) of ethyl 3-amino-2-benzo[b]furancarboxylate (EP 187487 A1) in 10 mL of N,N-dimethylformamide dimethyl acetal is heated at reflux temperature for 1.5 hours, then cooled to room temperature and concentrated in vacuo. The residue is partitioned between ethyl acetate and water. The organic layer is washed with water, dried over sodium sulfate, passed through a pad of diatomaceous earth and concentrated in vacuo. The solid is collected by filtration to provide 3.90 g (75%) of a white solid, mp 89–90° C.;

후처리

  1. temperatureis heated
  2. temperatureat reflux temperature for 1.5 hours
  3. concentrationconcentrated in vacuo
  4. customThe residue is partitioned between ethyl acetate and water
  5. washThe organic layer is washed with water
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated in vacuo
  8. filtrationThe solid is collected by filtration

출처 및 근거

ORD 기록
ord-e6aec541f4d14e00ade674578fe2a4bb
출처 데이터셋
uspto-grants-2006_09
특허 번호
US07105531B2

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