Water → 3-[2-{(1R*,2R*)-2-hydroxy-2-methylcyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine

HRID 965351

反応式

HRID 965351 の反応式
[O:1]=[C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[N:10][N:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=23)=[N:4][NH:3]1.[CH3:23][C:24]12[O:30][CH:25]1[CH2:26][CH2:27][CH2:28][CH2:29]2.[OH-].[Na+].O>[Cl-].C([N+](C)(C)C)C1C=CC=CC=1.C1(C)C=CC=CC=1>[OH:30][C@:24]1([CH3:23])[CH2:29][CH2:28][CH2:27][CH2:26][C@H:25]1[N:3]1[C:2](=[O:1])[CH:7]=[CH:6][C:5]([C:8]2[C:9]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[N:10][N:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=23)=[N:4]1

参加物

7

実験手順

A mixture of 3-(3-oxo-2,3-dihydropyridazin-6-yl)-2-phenylpyrazolo[1,5-a]pyridine (2.25 g), 1-methyl-1,2-epoxycyclohexane (1.31 g), benzyltrimethylammonium chloride (178 mg), 1N aqueous sodium hydroxide (7.8 ml), water (17 ml), and toluene was heated to reflux for 8 hours and 20 minutes. After the reaction mixture was cooled to room temperature, the precipitates were collected by filtration, washed with water, and dried. The crude material was purified by column chromatography on silica gel (CH2Cl2 :EtOAc=10:2) to give colorless crystals of 3-[2-{(1R*,2R*)-2-hydroxy-2-methylcyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine (189 mg).

後処理

  1. temperaturewas heated
  2. temperatureto reflux for 8 hours and 20 minutes
  3. filtrationthe precipitates were collected by filtration
  4. washwashed with water
  5. customdried
  6. customThe crude material was purified by column chromatography on silica gel (CH2Cl2 :EtOAc=10:2)

出典と根拠

ORDレコード
ord-6e03ee8a66a946259afa79e1cb9fe6b6
出典データセット
uspto-grants-1998_06
特許番号
US05773530

関連ノート

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