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7-Benzyl-hexahydro-oxazolo[3,4-a]pyrazin-3-one → Tetrahydro-1H-oxazolo[3,4-a]pyrazin-3(5H)-one

HRID 1972723
ノート
印刷プレビュー

反応式

HRID 1972723 の反応式
C([N:8]1[CH2:13][CH2:12][N:11]2[C:14](=[O:17])[O:15][CH2:16][CH:10]2[CH2:9]1)C1C=CC=CC=1>[Pd].CCO>[CH2:16]1[CH:10]2[CH2:9][NH:8][CH2:13][CH2:12][N:11]2[C:14](=[O:17])[O:15]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 1

HCID 591357857-Benzyl-hexahydro-oxazolo[3,4-a]pyrazin-3-one

生成物 1

HCID 22562207Tetrahydro-1H-oxazolo[3,4-a]pyrazin-3(5H)-one収率 97%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒2 回

実験手順

10% Palladium on carbon (18 mg, 20% by wt.) was placed under an inert atmosphere and suspended in EtOH (1 mL). A solution of 7-benzyl-hexahydro-oxazolo[3,4-a]pyrazin-3-one (90 mg, 0.39 mmol) dissolved in EtOH (3.8 mL) was added. The reaction mixture was placed under H2 atmosphere (1 atmosphere pressure) and stirred overnight. The resulting mixture was filtered through a pad of Celite® and the solvent was concentrated in vacuo to give 53.6 mg (97%) of the title compound as clear oil. 1H-NMR (300 MHz, CD3Cl) 4.36 (t, 1H), 3.89 to 3.81 (m, 1H), 3.79 to 3.69 (m, 2H), 3.10 to 2.88 (m, 3H), 2.67 to 2.50 (m, 2H), 2.00 to 1.90 (m, 1H).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. additionwas added
  2. filtrationThe resulting mixture was filtered through a pad of Celite®
  3. concentrationthe solvent was concentrated in vacuo

出典と根拠

ORDレコード
ord-07d93527068e418dad8a76e54b7170a2
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08431695B2

反応ノート

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