Aluminum(III) Chloride → 6-Hydroxy-4-(4-methoxyanilino)-7-methyl-1,8-naphthyridine-3-carboxylic acid hemihydrate

HRID 128634

반응식

HRID 128634 반응식
[CH3:1][O:2][C:3]1[CH:28]=[CH:27][C:6]([NH:7][C:8]2[C:17]3[C:12](=[N:13][C:14]([CH3:21])=[C:15]([O:18]CC)[CH:16]=3)[N:11]=[CH:10][C:9]=2[C:22]([O:24]CC)=[O:23])=[CH:5][CH:4]=1.[Cl-].[Al+3].[Cl-].[Cl-]>ClCCl>[OH2:2].[OH:18][C:15]1[CH:16]=[C:17]2[C:12](=[N:13][C:14]=1[CH3:21])[N:11]=[CH:10][C:9]([C:22]([OH:24])=[O:23])=[C:8]2[NH:7][C:6]1[CH:27]=[CH:28][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1.[OH:18][C:15]1[CH:16]=[C:17]2[C:12](=[N:13][C:14]=1[CH3:21])[N:11]=[CH:10][C:9]([C:22]([OH:24])=[O:23])=[C:8]2[NH:7][C:6]1[CH:27]=[CH:28][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1

참가 물질

4

실험 절차

A mixture of ethyl 4-(4-methoxyanilino)-6-ethoxy-7-methyl-1,8-naphthyridine-3-carboxylate (2.9 g) in dichloromethane (45 ml) was added rapidly to a suspension of powdered anhydrous aluminium chloride (12.8 g) in dichloromethane (115 ml) with stirring. The mixture was stirred for 24 hours at ambient temperature and then poured into ice/water. The mixture was stirred for 30 minutes then filtered. The residue was basified and partitioned between dichloromethane and water. The aqueous layer was evaporated to dryness. The residue was dissolved in propan-2-ol (150 ml) and then purified by column chromatography to give 6-hydroxy-4-(4-methoxyanilino)-7-methyl-1,8-naphthyridine-3-carboxylic acid hemihydrate, m.p. 267°-268° C. (with decomposition).

후처리

  1. stirringThe mixture was stirred for 24 hours at ambient temperature
  2. stirringThe mixture was stirred for 30 minutes
  3. filtrationthen filtered
  4. custompartitioned between dichloromethane and water
  5. customThe aqueous layer was evaporated to dryness
  6. dissolutionThe residue was dissolved in propan-2-ol (150 ml)
  7. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-e25a5979be754341adcd7bb4818aa142
출처 데이터셋
uspto-grants-1995_11
특허 번호
US05464781

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