Dimethylformamide → 3-[(8-Acetamidoquinoline-5-sulfonyl)methyl]phenyl acetate

HRID 904723

反応式

HRID 904723 の反応式
[C:1]([NH:4][C:5]1[C:14]2[N:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:8]([S:15]([OH:17])=[O:16])=[CH:7][CH:6]=1)(=[O:3])[CH3:2].[C:18]([O:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([CH2:28]Br)[CH:23]=1)(=[O:20])[CH3:19].C(=O)(O)[O-].[Na+].CN(C)C=O>O>[C:1]([NH:4][C:5]1[CH:6]=[CH:7][C:8]([S:15]([CH2:28][C:24]2[CH:25]=[CH:26][CH:27]=[C:22]([O:21][C:18](=[O:20])[CH3:19])[CH:23]=2)(=[O:17])=[O:16])=[C:9]2[C:14]=1[N:13]=[CH:12][CH:11]=[CH:10]2)(=[O:3])[CH3:2]

参加物

6

実験手順

8-Acetamido-5-quinolinesulfinic acid (10 g, 40 mmole), m-(bromomethyl)phenyl acetate (11 g, 44 mmole), excess sodium bicarbonate (5 g) and dry dimethylformamide (50 ml) were mixed and heated on the steam bath for 11/2 hours. The mixture was slowly poured into 800 ml stirred water and the mixture stirred another 30 min. The solid was filtered off, washed with water, and air-dried overnight. Yield 15.8 g (99 percent) of crude but relatively pure product, m.p. 179°-182° C. A sample recrystallized from toluene, melted 180°-182° C.

後処理

  1. temperatureheated on the steam bath for 11/2 hours
  2. additionThe mixture was slowly poured into 800 ml
  3. filtrationThe solid was filtered off
  4. washwashed with water
  5. customair-dried overnight
  6. customA sample recrystallized from toluene
  7. custommelted 180°-182° C.

出典と根拠

ORDレコード
ord-abb3f45e76e34738869da91aab2f539b
出典データセット
uspto-grants-1983_12
特許番号
US04419435

関連ノート

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