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Thionyl Chloride → 4-Bromothiazole-2-carbohydrazide

HRID 1423334
ノート
印刷プレビュー

反応式

HRID 1423334 の反応式
[Br:1][C:2]1[N:3]=[C:4]([C:7]([OH:9])=O)[S:5][CH:6]=1.S(Cl)(Cl)=O.O.[NH2:15][NH2:16]>CO>[Br:1][C:2]1[N:3]=[C:4]([C:7]([NH:15][NH2:16])=[O:9])[S:5][CH: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 24386Thionyl ChlorideHCID 24654Hydrazine hydrate (1:1)HCID 151220654-Bromo-1,3-thiazole-2-carboxylic acid

生成物 1

HCID 580356604-Bromothiazole-2-carbohydrazide収率 78.1%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 4-bromothiazole-2-carboxylic acid (2.0 g, 9.8 mmol) in methanol (10 mL) was added thionyl chloride (710 μL, 9.8 mmol) and the mixture was refluxed for 3 hours. The solvent was removed under reduced pressure, and the residue was suspended in ethanol (10 mL). To this suspension was added hydrazine hydrate (2.4 mL, 49 mmol), and the reaction was heated to reflux for 90 minutes. The solvent was removed under reduced pressure, and the residue suspended in acetonitrile, filtered, and the solids were washed with acetonitrile, diethyl ether, and dried under vacuum to afford 1.7 g (77%) of 4-bromothiazole-2-carbohydrazide as a yellow solid. M+1=222.1

後処理

  1. temperaturethe mixture was refluxed for 3 hours
  2. customThe solvent was removed under reduced pressure
  3. temperaturethe reaction was heated
  4. temperatureto reflux for 90 minutes
  5. customThe solvent was removed under reduced pressure
  6. filtrationfiltered
  7. washthe solids were washed with acetonitrile, diethyl ether
  8. customdried under vacuum

出典と根拠

ORDレコード
ord-d37f4317650e4463abaf8fd96d5acf43
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08927582B2

反応ノート

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