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Semicarbazide hydrochloride → 6-(4-Fluorophenyl)-1,2,4-triazin-3(2H)-one

HRID 1099033
ノート
印刷プレビュー

反応式

HRID 1099033 の反応式
C(O[CH:4](OCC)[C:5]([C:7]1[CH:12]=[CH:11][C:10]([F:13])=[CH:9][CH:8]=1)=O)C.Cl.[NH2:18][NH:19][C:20]([NH2:22])=[O:21]>C(O)C>[F:13][C:10]1[CH:9]=[CH:8][C:7]([C:5]2[CH:4]=[N:22][C:20](=[O:21])[NH:19][N:18]=2)=[CH:12][CH:11]=1
参加物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 11236Semicarbazide hydrochlorideHCID 224161332,2-Diethoxy-1-(4-fluorophenyl)ethanone

生成物 1

HCID 125812846-(4-Fluorophenyl)-1,2,4-triazin-3(2H)-one

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A mixture of 2,2-diethoxy-1-(4-fluorophenyl)ethanone (5.15 g, 0.0228 mol), semicarbazide hydrochloride (2.6 g, 0.024 mol) in ethanol (50 mL) was stirred at RT overnight, and then heated at 80° C. for 5 h. The mixture was concentrated. The residue was dissolved in acetic acid (50 mL), and heated at 130° C. for 6 h. After cooling, the mixture was concentrated, and the residue was triturated with ethyl ether, filtered, and washed with ether and then hexane. The crystalline solid was collected and dried under high vacuum to the desired product (4.18 g, 96.1%). Analytical LCMS: (M+H)+=192.1.

後処理

  1. temperatureheated at 80° C. for 5 h
  2. concentrationThe mixture was concentrated
  3. dissolutionThe residue was dissolved in acetic acid (50 mL)
  4. temperatureheated at 130° C. for 6 h
  5. temperatureAfter cooling
  6. concentrationthe mixture was concentrated
  7. customthe residue was triturated with ethyl ether
  8. filtrationfiltered
  9. washwashed with ether
  10. customThe crystalline solid was collected
  11. dry with materialdried under high vacuum to the desired product (4.18 g, 96.1%)

出典と根拠

ORDレコード
ord-c89c9e231b4f4bcaa3f1923e89ae249f
出典データセット
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08143251B2

反応ノート

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