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1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 56592712、化合物

HRID 2359274
ノート
印刷プレビュー

反応式

HRID 2359274 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[S:9][C:10]1[CH:18]=[CH:17][C:13]([C:14](O)=[O:15])=[CH:12][CH:11]=1.C(N=C=NCCCN(C)C)C.[CH3:30][S:31]([NH2:34])(=[O:33])=[O:32]>CN(C)C1C=CN=CC=1.CN(C)C=O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[S:9][C:10]1[CH:18]=[CH:17][C:13]([C:14]([NH:34][S:31]([CH3:30])(=[O:33])=[O:32])=[O:15])=[CH:12][CH:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 72879MethanesulfonamideHCID 112654344-[(2-Methoxyphenyl)thio]benzoic acid

生成物 1

HCID 56592712HCID 56592712、化合物収率 30.9%

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 6228
Dimethylformamide
溶媒

実験手順

4-(2-methoxyphenylthio)benzoic acid (126 mg, 0.48 mmol), 4-dimethylaminopyridine (12.2 mg, 0.10 mmol) and 1-ethyl-3-(dimethylaminopropyl)carbodiimide (195 mg, 0.97 mmol) were dissolved in anhydrous N,N-dimethylformamide (4 mL) and stirred for 60 minutes. To this solution was added methanesulphonamide (70 mg, 0.72 mmol) and the reaction mixture was stirred at room temperature for 18 hours. The reaction was quenched by the addition of water (10 mL) and the mixture extracted with ethyl acetate (3×10 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give 50 mg of a crude oil which was purified by preparative HPLC title compound.

後処理

  1. stirringthe reaction mixture was stirred at room temperature for 18 hours
  2. customThe reaction was quenched by the addition of water (10 mL)
  3. extractionthe mixture extracted with ethyl acetate (3×10 mL)
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-fd96fa0cd21a4d1d927d531b3af242be
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08685977B2

反応ノート

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