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Morpholine → 1,4-Dimorpholino-7-phenylpyrido(3,4-d)pyridazine

HRID 1604903
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HRID 1604903 반응식
CS[C:3]1[N:8]=[N:7][C:6](SC)=[C:5]2[CH:11]=[N:12][C:13]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)=[CH:14][C:4]=12.[NH:21]1[CH2:26][CH2:25][O:24][CH2:23][CH2:22]1>>[O:24]1[CH2:25][CH2:26][N:21]([C:3]2[N:8]=[N:7][C:6]([N:21]3[CH2:26][CH2:25][O:24][CH2:23][CH2:22]3)=[C:5]3[CH:11]=[N:12][C:13]([C:15]4[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=4)=[CH:14][C:4]=23)[CH2:22][CH2:23]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 8083MorpholineHCID 12246673HCID 12246673, 화합물

생성물 1

HCID 1004941,4-Dimorpholino-7-phenylpyrido(3,4-d)pyridazine

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온도
180 °C

실험 절차

1 part by weight of 1,4-dimethylmercapto-7-phenylpyrido[3,4-d]pyridazine and 10 parts by volume of morpholine are placed in a glass tube, and the glass tube is sealed. The reaction system is heated at 180°C for 8 hours. The excess amount of morpholine is removed by evaporating under reduced pressure, and water is added to the residue. Thus precipitated crude crystals are collected by filtration. The crude crystals are adsorbed on a column packed with silica-gel, followed by eluting with a mixture of acetone and benzene (1:4). The eluate is concentrated under reduced pressure and recrystallized from methanol to obtain 1,4-dimorpholino-7-phenylpyrido[3,4-d]pyridazine as pale yellow needles melting at 186° to 188°C.

후처리

  1. customthe glass tube is sealed
  2. customThe excess amount of morpholine is removed
  3. customby evaporating under reduced pressure, and water
  4. additionis added to the residue
  5. customThus precipitated crude crystals
  6. filtrationare collected by filtration
  7. washby eluting with a mixture of acetone and benzene (1:4)
  8. concentrationThe eluate is concentrated under reduced pressure
  9. customrecrystallized from methanol

출처 및 근거

ORD 기록
ord-c11001a614ff4854af63ac55490459ef
출처 데이터셋
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03948908

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