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HCID 23121865、化合物 → Hexahydro-1,1-dimethyl-3H-oxazolo[3,4-A]pyrazin-3-one

HRID 1713481
ノート
印刷プレビュー

反応式

HRID 1713481 の反応式
C1(COC([N:11]2[CH2:16][CH2:15][N:14]3[C:17](=[O:22])[O:18][C:19]([CH3:21])([CH3:20])[CH:13]3[CH2:12]2)=O)C=CC=CC=1>C(O)C.[C].[Pd]>[CH3:20][C:19]1([CH3:21])[CH:13]2[CH2:12][NH:11][CH2:16][CH2:15][N:14]2[C:17](=[O:22])[O:18]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 23121865HCID 23121865、化合物

生成物 1

HCID 23122055Hexahydro-1,1-dimethyl-3H-oxazolo[3,4-A]pyrazin-3-one収率 73%

試薬・触媒・溶媒 2

HCID 178418390HCID 178418390、化合物触媒HCID 702Ethanol溶媒

実験手順

(Phenylmethyl)tetrahydro-3-oxo-1,1-dimethyl-3H-oxazolo[3,4-a]pyrazine-7(1H)-carboxylate (0.97 g, 3.2 mmol) was dissolved in ethanol (50 mL). 10% Palladium carbon (0.10 g) was added thereto, and the resulting mixture was stirred under hydrogen atmosphere at room temperature one whole day and night. The reaction solution was filtered through a Celite, and the Celite was washed with ethanol. The filtrate was concentrated under reduced pressure and left to stand at room temperature overnight. The resulting crystals were collected by filtration and washed with diethyl ether to obtain the title compound (0.39 g, yield 73%).

後処理

  1. filtrationThe reaction solution was filtered through a Celite
  2. washthe Celite was washed with ethanol
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. waitleft
  5. filtrationThe resulting crystals were collected by filtration
  6. washwashed with diethyl ether

出典と根拠

ORDレコード
ord-3f31592aff7540e3aa26d3a94fc354f5
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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