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Hydrochloric Acid → 4-[(Dimethylsulfamoyl)amino]-N-phenylbenzamide

HRID 1982279
ノート
印刷プレビュー

反応式

HRID 1982279 の反応式
[NH2:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[O:7])=[CH:4][CH:3]=1.[CH3:17][N:18]([CH3:23])[S:19](Cl)(=[O:21])=[O:20].Cl>N1C=CC=CC=1>[CH3:17][N:18]([CH3:23])[S:19]([NH:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[O:7])=[CH:4][CH:3]=1)(=[O:21])=[O:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 699104-Amino-N-phenylbenzamideHCID 83372Dimethylsulphamoyl chloride

生成物 1

HCID 133219734-[(Dimethylsulfamoyl)amino]-N-phenylbenzamide収率 57.4%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

To a solution of 1.0 g of 4-aminobenzanilide 4 dissolved in 10 ml of dried pyridine is added 1.01 g of dimethylaminosulfonyl chloride 5 at room temperature, and the mixture is stirred over-night. The reaction mixture is poured into ice-water, acidified with 6N hydrochloric acid, and extracted with a mixture of methylene chloride-methanol. The organic layer is extracted again with 10% sodium hydroxide solution. The alkaline layer is acidified with 6N hydrochloric acid; the precipitate is collected by filtration and recrystallized from methanol to give 864 mg of 4-[(dimethylaminosulfonyl)amino]benzanilide 6 as crystals, m.p. 213°-215° C.

後処理

  1. extractionextracted with a mixture of methylene chloride-methanol
  2. extractionThe organic layer is extracted again with 10% sodium hydroxide solution
  3. filtrationthe precipitate is collected by filtration
  4. customrecrystallized from methanol

出典と根拠

ORDレコード
ord-fe6216b011ca456882813f5f470d7872
出典データセット
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04595780

反応ノート

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