Acetic Anhydride → HCID 136199666, 화합물

HRID 263570노트

반응식

HRID 263570 반응식
[C:1]1([C:7]2[N:8]=[C:9]([C:12]3[CH:13]=[N+:14]([O-])[CH:15]=[CH:16][CH:17]=3)[S:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(OC(=O)C)(=[O:21])C>>[O:21]=[C:13]1[C:12]([C:9]2[S:10][CH:11]=[C:7]([C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)[N:8]=2)=[CH:17][CH:16]=[CH:15][NH:14]1

참가 물질

3

반응물 2

HCID 7918Acetic AnhydrideHCID 187071743-(4-phenylthiazol-2-yl)pyridine-N-oxide

생성물 1

HCID 136199666HCID 136199666, 화합물

실험 절차

In 25 ml of acetic anhydride was dissolved 2.8 g of 3-(4-phenylthiazol-2-yl)pyridine-N-oxide. The solution was refluxed for 6 hours with heating. The solvent was removed by distillation. The residue was treated with ammonia water and extracted with dichloromethane. The extract was water-washed, dried and subjected to solvent removal by distillation. The residue was mixed with a small amount of dichloromethane. The resulting crystals were collected by filtration and recrystallized from methanol to obtain 60 mg of 2-(2-oxopyridin-3-yl)4-phenylthiazole as light brown plate crystals.

후처리

  1. temperatureThe solution was refluxed for 6 hours
  2. temperaturewith heating
  3. customThe solvent was removed by distillation
  4. additionThe residue was treated with ammonia water
  5. extractionextracted with dichloromethane
  6. washwashed
  7. customdried
  8. customsubjected to solvent removal by distillation
  9. additionThe residue was mixed with a small amount of dichloromethane
  10. filtrationThe resulting crystals were collected by filtration
  11. customrecrystallized from methanol

출처 및 근거

ORD 기록
ord-ca93c77a03fc4ab6a8c39369d389e9f7
출처 데이터셋
uspto-grants-1997_07
특허 번호
US05643932

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