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Butyryl chloride → HCID 54096992、化合物

HRID 1390082
ノート
印刷プレビュー

反応式

HRID 1390082 の反応式
O.Cl.Cl.[NH2:4][C:5]1[CH:6]=[C:7]([CH:12]=[C:13]([S:22](=[O:25])(=[O:24])[NH2:23])[C:14]=1[CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[CH2:8][N:9]([CH3:11])[CH3:10].N[C:27]1[CH:28]=C(C=[C:35](S(=O)(=O)N)[C:36]=1CC1C=CC=CC=1)CN(C)C.Cl.Cl.[OH-].[Na+].CCCC(Cl)=O.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C(Cl)Cl.COCCOC.O.C(OCC)(=O)C>[CH2:15]([C:14]1[C:13]([S:22](=[O:25])(=[O:24])[NH2:23])=[CH:12][C:7]([CH2:8][N:9]([CH3:10])[CH3:11])=[CH:6][C:5]=1[NH:4][CH2:28][CH2:27][CH2:36][CH3:35])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 4

HCID 8855Butyryl chlorideHCID 14798Sodium HydroxideHCID 21226445Aluminium lithium hydrideHCID 70574148HCID 70574148、化合物

生成物 1

HCID 54096992HCID 54096992、化合物

試薬・触媒・溶媒 4

HCID 962Water溶媒
HCID 6344
Dichloromethane
溶媒
2 回
HCID 80711,2-Dimethoxyethane溶媒2 回
HCID 8857Ethyl Acetate溶媒

実験手順

To a vigorously stirred mixture of (3-amino-4-benzyl-5-sulfamylbenzyl)dimethylamine dihydrochloride hemihydrate (4.0 g; prepared as described in Example 209), 2 N sodium hydroxide (60 ml) and methylene chloride (40 ml) a solution of n-butyryl chloride (1.1 g) in methylene chloride (12 ml) is dropwise added during 30 minutes keeping the temperature at 0°-5° C. by external cooling. After additional stirring at 22°-25° C. for 2 hours, the organic layer is separated, washed with water and dried in the presence of magnesium sulphate. The methylene chloride is then removed in vacuo to yield crude (4-benzyl-3-n-butyrylamido-5-sulfamylbenzyl)dimethylamine as an oil. The crude amine is dissolved in dry 1,2-dimethoxyethane (50 ml) and the resulting solution is dropwise added at 100° C. during 45 minutes to a stirred mixture of lithium aluminium hydride (2.0 g) and 1,2-dimethoxyethane (40 ml). After additional refluxing and stirring for 16 hours, the mixture is cooled, and ethyl acetate (4 ml) followed by water (8 ml) are very cautiously added. The mixture is stirred for a further 30 minutes and is then heated on a steam-bath and filtered hot. The filtercake is carefully washed with hot 1,2-dimethoxyethane (3 portions of 25 ml), whereafter the combined filtrates are evaporated in vacuo to yield crude (4-benzyl-3-n-butylamino-5-sulfamylbenzyl)dimethylamine. After recrystallization from ethanol it is obtained with a melting point of 111°-113° C. The material (IR, analysis) is identical with the material prepared as in Example 172.

後処理

  1. additionis dropwise added during 30 minutes
  2. customat 0°-5° C.
  3. customthe organic layer is separated
  4. washwashed with water
  5. dry with materialdried in the presence of magnesium sulphate
  6. customThe methylene chloride is then removed in vacuo
  7. customto yield crude (4-benzyl-3-n-butyrylamido-5-sulfamylbenzyl)dimethylamine as an oil
  8. temperatureAfter additional refluxing
  9. stirringstirring for 16 hours
  10. temperaturethe mixture is cooled
  11. additionare very cautiously added
  12. stirringThe mixture is stirred for a further 30 minutes
  13. temperatureis then heated on a steam-bath
  14. filtrationfiltered hot
  15. washThe filtercake is carefully washed with hot 1,2-dimethoxyethane (3 portions of 25 ml), whereafter the combined filtrates
  16. customare evaporated in vacuo

出典と根拠

ORDレコード
ord-9d28b882ea4b4f0a9f43bb3f82b749a3
出典データセット
uspto-grants-1981_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04247550

反応ノート

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