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Isopropanol → HCID 178459484、化合物

HRID 1954742
ノート
印刷プレビュー

反応式

HRID 1954742 の反応式
[Cl:1][C:2]1[CH:22]=[CH:21][C:5]2[C:6](=[O:20])[C:7]3[C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[N:13][NH:12][C:8]=3[C:9](=[O:11])[NH:10][C:4]=2[CH:3]=1.[CH3:23]C(O)C>Cl>[Cl:1][C:2]1[CH:22]=[CH:21][C:5]2[C:6](=[O:20])[C:7]3[C:14]([C:15]([O:17][CH:18]([CH3:23])[CH3:19])=[O:16])=[N:13][NH:12][C:8]=3[C:9](=[O:11])[NH:10][C:4]=2[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 3776IsopropanolHCID 1784704817-Chloro-3-(ethoxycarbonyl)pyrazolo[3,4-c][1]benzazepine-4,10-(1H,9H)dione

生成物 1

HCID 178459484HCID 178459484、化合物収率 48%

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid触媒

実験手順

A solution of 7-chloro-3-(ethoxycarbonyl)pyrazolo[3,4-c][1]benzazepine-4,10(1H,9H)-dione (500 mg, 1.56 mmol), 2-propanol (60 mL), and concentrated hydrochloric acid (3 drops) was subjected to three cycles of partial solvent removal by slow distillation (over 6 hours) followed by overnight reflux. After the third cycle, solvent was removed by rotary evaporation and the crude product was purified by flash chromatography eluting with dichloromethane:2-propanol (95:5-85:15) to yield the title compound as a white solid (256 mg, 48%, m.p. 291° C). Alternatively, the title compound can be prepared as described in Example 18 shown hereinbelow in Table 1.

後処理

  1. temperaturereflux
  2. customAfter the third cycle, solvent was removed by rotary evaporation
  3. customthe crude product was purified by flash chromatography
  4. washeluting with dichloromethane:2-propanol (95:5-85:15)

出典と根拠

ORDレコード
ord-0bea96bc1f4340cb9dd29795c317afc6
出典データセット
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06124281

反応ノート

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