Ammonia → 4-Isopropoxy-3-thioureidobenzenesulfonamide

HRID 333587ノート

反応式

HRID 333587 の反応式
[CH:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([S:11]([NH2:14])(=[O:13])=[O:12])=[CH:7][C:6]=1[N:15]=[C:16]=[S:17])([CH3:3])[CH3:2].[NH3:18]>CO>[CH:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([S:11]([NH2:14])(=[O:13])=[O:12])=[CH:7][C:6]=1[NH:15][C:16]([NH2:18])=[S:17])([CH3:3])[CH3:2]

参加物

4

反応物 2

HCID 222AmmoniaHCID 866653704-Isopropoxy-3-isothiocyanato-benzenesulfonamide

生成物 1

HCID 866655834-Isopropoxy-3-thioureidobenzenesulfonamide

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Crude 4-isopropoxy-3-isothiocyanato-benzenesulfonamide (17.8 g, 65.2 mmol, example 2, step e) was treated with a 2 M solution of ammonia in MeOH (250 mL) and the resulting solution was stirred at room temperature for 18 h. The reaction mixture was then concentrated to about half the volume until a large amount of tan solid precipitated. The suspension was cooled to 0° C. for 30 minutes and was filtered. The solid was washed with methanol and ether to give the title compound as a cream colored solid.

後処理

  1. concentrationThe reaction mixture was then concentrated to about half the volume until a large amount of tan solid
  2. customprecipitated
  3. temperatureThe suspension was cooled to 0° C. for 30 minutes
  4. filtrationwas filtered
  5. washThe solid was washed with methanol and ether

出典と根拠

ORDレコード
ord-70c80e45bdf347d09656aac61a11f388
出典データセット
uspto-grants-2014_11
特許番号
US08883473B2

反応ノート

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