Dimethylamine → 2-Oxo-2,3-dihydro-1H-indole-5-sulfonic acid dimethylamide

HRID 49119

反応式

HRID 49119 の反応式
Cl[S:2]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[NH:10][C:9](=[O:14])[CH2:8]2)(=[O:4])=[O:3].[CH3:15][NH:16][CH3:17]>CO>[CH3:15][N:16]([CH3:17])[S:2]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[NH:10][C:9](=[O:14])[CH2:8]2)(=[O:4])=[O:3]

参加物

4

反応物 2

HCID 674DimethylamineHCID 49625062-oxo-2,3-dihydro-1H-indole-5-sulfonyl chloride

生成物 1

HCID 98161852-Oxo-2,3-dihydro-1H-indole-5-sulfonic acid dimethylamide収率 79%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A suspension of 2.3 g of 5-chlorosulfonyl-2-oxindole in 10 mL of 2M dimethylamine in methanol was stirred at room temperature for 4 hours at which time a white solid was present. The precipitate was collected by vacuum filtration, washed with 5 mL of 1N sodium hydroxide and 5 mL of 1N hydrochloric acid and dried under vacuum at 40° C. overnight to give 1.9 g (79 % yield) of 5-dimethylaminosulfonyl-2-oxindole.

後処理

  1. filtrationThe precipitate was collected by vacuum filtration
  2. washwashed with 5 mL of 1N sodium hydroxide and 5 mL of 1N hydrochloric acid
  3. customdried under vacuum at 40° C. overnight

出典と根拠

ORDレコード
ord-7bcb2d7ac49545c89c9ba19bf5d8cc73
出典データセット
uspto-grants-2004_03
特許番号
US06706709B2

関連ノート

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