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

HRID 1713481
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HRID 1713481 반응식
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
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참가 물질

4

반응물 1

HCID 23121865HCID 23121865, 화합물

생성물 1

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

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 702Ethanol용매

실험 절차

(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%).

후처리

  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

출처 및 근거

ORD 기록
ord-3f31592aff7540e3aa26d3a94fc354f5
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07795267B2

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