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Potassium Carbonate → HCID 178513412、化合物

HRID 604484
ノート
印刷プレビュー

反応式

HRID 604484 の反応式
[NH2:1][C:2]1[S:3][C:4]([C:13]#[N:14])=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:6]=1.Cl.[NH2:16][OH:17].C(=O)([O-])[O-].[K+].[K+]>O.C(O)C>[NH2:1][C:2]1[S:3][C:4]([C:13]([NH:16][OH:17])=[NH:14])=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:6]=1
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 11430Potassium CarbonateHCID 443297Hydroxyamine hydrochlorideHCID 214555522-Amino-4-Phenylthiazole-5-carbonitrile

生成物 1

HCID 178513412HCID 178513412、化合物

試薬・触媒・溶媒 1

HCID 19096565Water ethanol溶媒

実験手順

2-Amino-4-phenyl-thiazole-5-carbonitrile (0.13 g, 0.6 mmol) was suspended in 1:1 water/ethanol (v/v) (24 mL) and added hydroxylamine hydrochloride (1.47 g, 21 mmol) and potassium carbonate (1.86 g, 13 mmol). The reaction mixture was heated at reflux for 3 days, then the solvent was reduced and the aqueous phase was extracted with dichloromethane. The organic layer was washed with water and brine, and was dried over sodium sulfate. The solvent was evaporated to yield a yellow solid. Yield: 0.1 g, 66%.

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. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 3 days
  3. extractionthe aqueous phase was extracted with dichloromethane
  4. washThe organic layer was washed with water and brine
  5. dry with materialwas dried over sodium sulfate
  6. customThe solvent was evaporated
  7. customto yield a yellow solid

出典と根拠

ORDレコード
ord-919aa211b7e649a5998c567356593ff2
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07910613B2

反応ノート

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