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Hydrazine hydrate (1:1) → 2-Amino-4-cyclopropyl-1,3-thiazole-5-carbohydrazide

HRID 389099
ノート
印刷プレビュー

反応式

HRID 389099 の反応式
Br.[NH2:2][C:3]1[S:4][C:5]([C:11]([O:13]C)=O)=[C:6]([CH:8]2[CH2:10][CH2:9]2)[N:7]=1.O.[NH2:16][NH2:17]>CO>[NH2:2][C:3]1[S:4][C:5]([C:11]([NH:16][NH2:17])=[O:13])=[C:6]([CH:8]2[CH2:10][CH2:9]2)[N:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 86653012Methyl 2-amino-4-cyclopropyl-1,3-thiazole-5-carboxylate hydrobromide

生成物 1

HCID 582439332-Amino-4-cyclopropyl-1,3-thiazole-5-carbohydrazide

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
55 °C

実験手順

Methyl 2-amino-4-cyclopropyl-1,3-thiazole-5-carboxylate hydrobromide (1.78 g) was dissolved in methanol (4.0 ml), hydrazine monohydrate (2.0 ml) was added thereto, followed by stirring at 55° C. for 3 days. After cooling to room temperature, an insoluble substance was filtered, the mother solution was mixed with basic silica gel and the solvent was evaporated under reduced pressure. The residue was purified by basic silica gel chromatography (chloroform:methanol) to obtain, as a dark brown solid, 2-amino-4-cyclopropyl-1,3-thiazole-5-carbohydrazide (224 mg).

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureAfter cooling to room temperature
  2. filtrationan insoluble substance was filtered
  3. additionthe mother solution was mixed with basic silica gel
  4. customthe solvent was evaporated under reduced pressure
  5. customThe residue was purified by basic silica gel chromatography (chloroform:methanol)

出典と根拠

ORDレコード
ord-309afcba4bca442eb3f07c12bba5c19f
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08377923B2

反応ノート

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