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Methylamine → N-(3-fluoro-4-methylsulfamoylphenyl)acetamide

HRID 1959788
ノート
印刷プレビュー

反応式

HRID 1959788 の反応式
[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([S:11](Cl)(=[O:13])=[O:12])=[C:7]([F:15])[CH:6]=1)(=[O:3])[CH3:2].[CH3:16][NH2:17]>ClCCl.C1COCC1>[F:15][C:7]1[CH:6]=[C:5]([NH:4][C:1](=[O:3])[CH3:2])[CH:10]=[CH:9][C:8]=1[S:11](=[O:13])(=[O:12])[NH:17][CH3:16]
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 2

HCID 6329MethylamineHCID 167710844-Acetamido-2-fluorobenzene-1-sulfonyl chloride

生成物 1

HCID 34029456N-(3-fluoro-4-methylsulfamoylphenyl)acetamide収率 79%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

The above prepared 4-acetylamino-2-fluorobenzenesulfonyl chloride (2 g, 7.9 mmol) was dissolved in dichloromethane and methylamine (9.9 mL of a 2M solution in THF, 19.9 mmol) was added. The reaction was stirred at room temperature for 2 hrs. The solvent was then evaporated under reduced pressure and the resulting solid was suspended in 50 mL of water. The solid was isolated by filtration and dried to yield 1.55 g (79%) of N-(3-fluoro-4-methylsulfamoylphenyl)acetamide which was used in the subsequent step without further purification.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customThe solvent was then evaporated under reduced pressure
  2. customThe solid was isolated by filtration
  3. customdried

出典と根拠

ORDレコード
ord-932d7b0f04ce4c569838cc881a082d45
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08410272B2

反応ノート

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