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Benzamide → N-Benzoyl-tetrahydro-3-oxo-1,1-diphenyl-3H-oxazolo[3,4-a]pyrazine-7(1H)-carboxamide

HRID 1713531
ノート
印刷プレビュー

反応式

HRID 1713531 の反応式
[C:1]([NH2:9])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(Cl)(=O)[C:11](Cl)=[O:12].[C:16]1([C:22]2([C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)[CH:26]3[CH2:27][NH:28][CH2:29][CH2:30][N:25]3[C:24](=[O:31])[O:23]2)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>ClCCCl>[C:1]([NH:9][C:11]([N:28]1[CH2:29][CH2:30][N:25]2[C:24](=[O:31])[O:23][C:22]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)([C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=3)[CH:26]2[CH2:27]1)=[O:12])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=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

5

反応物 3

HCID 2331BenzamideHCID 65578Oxalyl chlorideHCID 231218811,1-Diphenyltetrahydro-1H-oxazolo[3,4-a]pyrazin-3(5H)-one

生成物 1

HCID 23121963N-Benzoyl-tetrahydro-3-oxo-1,1-diphenyl-3H-oxazolo[3,4-a]pyrazine-7(1H)-carboxamide収率 23.3%

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

反応条件

温度
90 °C

実験手順

Benzamide (1.0 g, 8.3 mmol) was dissolved in 1,2-dichloroethane (5 mL), oxalyl dichloride (1.2 g, 9.1 mmol) was added thereto, and the mixture was stirred at 90° C. for 30 hours. The reaction solution was concentrated under reduced pressure. Toluene (4 mL) was added thereto and dissolved. Hexahydro-1,1-diphenyl-3H-oxazolo[3,4-a]pyrazin-3-one (0.20 g, 0.68 mmol) was added thereto, and the mixture was stirred at 60° C. for 6 hours. The reaction solution was concentrated under reduced pressure to a half its original volume, and the precipitated crystals were filtered off. The residue was purified with silica gel column chromatography (hexane:ethyl acetate=1:1), and toluene (4 mL) was added thereto. The precipitated crystals were filtered off, and the filtrate was concentrated. The residue was further purified with silica gel column chromatography (hexane:ethyl acetate=1:1) and crystallized from diisopropyl ether to obtain the title compound (70 mg, yield 23%).

後処理

  1. concentrationThe reaction solution was concentrated under reduced pressure
  2. additionToluene (4 mL) was added
  3. dissolutiondissolved
  4. stirringthe mixture was stirred at 60° C. for 6 hours
  5. concentrationThe reaction solution was concentrated under reduced pressure to a half its original volume
  6. filtrationthe precipitated crystals were filtered off
  7. customThe residue was purified with silica gel column chromatography (hexane:ethyl acetate=1:1), and toluene (4 mL)
  8. additionwas added
  9. filtrationThe precipitated crystals were filtered off
  10. concentrationthe filtrate was concentrated
  11. customThe residue was further purified with silica gel column chromatography (hexane:ethyl acetate=1:1)
  12. customcrystallized from diisopropyl ether

出典と根拠

ORDレコード
ord-b16e9979b6494ab2a04385d37305622a
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07795267B2

反応ノート

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