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

HRID 500104
ノート
印刷プレビュー

反応式

HRID 500104 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 (5.2 g, 23 mmol), semicarbazide hydrochloride (2.6 g, 24 mmol) in ethanol (50 mL) was stirred overnight at ambient temperature and then heated to 80° C. for 5 hours. The reaction mixture was concentrated and the resulting residue was dissolved in acetic acid (50 mL) which was heated to 130° C. for 6 h. After cooling, the mixture was concentrated under reduced pressure. The residue was triturated with ethyl ether, filtered, and washed with diethyl ether and then hexanes. The crystalline material was collected and dried under high vacuum to give the desired product. (4.2 g, 96%) LCMS: (M+H)=192.1.

後処理

  1. temperatureheated to 80° C. for 5 hours
  2. concentrationThe reaction mixture was concentrated
  3. dissolutionthe resulting residue was dissolved in acetic acid (50 mL) which
  4. temperaturewas heated to 130° C. for 6 h
  5. temperatureAfter cooling
  6. concentrationthe mixture was concentrated under reduced pressure
  7. customThe residue was triturated with ethyl ether
  8. filtrationfiltered
  9. washwashed with diethyl ether
  10. customThe crystalline material was collected
  11. customdried under high vacuum

出典と根拠

ORDレコード
ord-7ef1b21d62884fc29070255c63f2aa87
出典データセット
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07767675B2

反応ノート

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