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Potassium Hydroxide → 2-Amino-6,7-dihydro-7-phenylcyclopent(e)-1,3-oxazin-4(5H)-one

HRID 474251
ノート
印刷プレビュー

反応式

HRID 474251 の反応式
S(O)(O)(=O)=O.CS[C:8](=[NH:10])[NH2:9].[OH-].[K+].[O:13]=[C:14]1[CH:18]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:17][CH2:16][CH:15]1[C:25](OCC)=[O:26]>O>[NH2:9][C:8]1[O:13][C:14]2[CH:18]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:17][CH2:16][C:15]=2[C:25](=[O:26])[N:10]=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 14797Potassium HydroxideHCID 752702-Methyl-2-thiopseudourea sulfateHCID 10561546Ethyl 2-oxo-3-phenylcyclopentanecarboxylate

生成物 1

HCID 53236142-Amino-6,7-dihydro-7-phenylcyclopent(e)-1,3-oxazin-4(5H)-one収率 61.2%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

2-Methyl-2-thiopseudourea sulfate (1.336 g, 9.61 mmol) was dissolved in water (10 mL) and KOH (1.128 g, 20.10 mmol) was added. While stirring, ethyl 2-oxo-3-phenylcyclopentanecarboxylate (2.03 g, 8.74 mmol) was added and the reaction mixture was stirred at room temperature overnight. The reaction mixture was filtered, washed with water and ether, and dried over anhydrous sodium sulfate to afford 2-amino-7-phenyl-6,7-dihydrocyclopenta[e][1,3]oxazin-4(5H)-one (1.22 g, 5.35 mmol, 61.2% yield) as white solid. LC-MS (M+H)+=229.1. 1H NMR (500 MHz, DMSO-d6) δ ppm 7.57-7.85 (2H, m), 7.08-7.47 (5H, m), 4.25-4.38 (1H, m), 1.72-2.73 (3H, m), 1.09-1.31 (1H, m).

後処理

  1. stirringthe reaction mixture was stirred at room temperature overnight
  2. filtrationThe reaction mixture was filtered
  3. washwashed with water and ether
  4. dry with materialdried over anhydrous sodium sulfate

出典と根拠

ORDレコード
ord-a304d809731d4e3b861941eb0e255d89
出典データセット
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08637523B2

反応ノート

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