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

HRID 389099
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HRID 389099 반응식
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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol용매

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온도
55 °C

실험 절차

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).

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후처리

  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)

출처 및 근거

ORD 기록
ord-309afcba4bca442eb3f07c12bba5c19f
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08377923B2

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