Benzyl [2,2-dimethyl-5-(5-methyl-1,3-oxazol-2-yl)-1,3-dioxan-5-yl]carbamate → 2,2-Dimethyl-5-(5-methyl-1,3-oxazol-2-yl)-1,3-dioxan-5-amine

HRID 923489노트

반응식

HRID 923489 반응식
[CH3:1][C:2]1([CH3:25])[O:7][CH2:6][C:5]([NH:14]C(=O)OCC2C=CC=CC=2)([C:8]2[O:9][C:10]([CH3:13])=[CH:11][N:12]=2)[CH2:4][O:3]1>C(O)C.[C].[Pd]>[CH3:1][C:2]1([CH3:25])[O:7][CH2:6][C:5]([C:8]2[O:9][C:10]([CH3:13])=[CH:11][N:12]=2)([NH2:14])[CH2:4][O:3]1

참가 물질

4

반응물 1

HCID 131734989Benzyl [2,2-dimethyl-5-(5-methyl-1,3-oxazol-2-yl)-1,3-dioxan-5-yl]carbamate

생성물 1

HCID 1183087412,2-Dimethyl-5-(5-methyl-1,3-oxazol-2-yl)-1,3-dioxan-5-amine수율 99.8%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 702Ethanol용매

실험 절차

To a solution of 35 mg of benzyl [2,2-dimethyl-5-(5-methyl-1,3-oxazol-2-yl)-1,3-dioxan-5-yl]carbamate in 2 ml of ethanol was added 10 mg of 10% palladium-carbon (hydrated), followed by stirring at room temperature for 4 hours under a hydrogen atmosphere of 1 atm. The reaction mixture was filtered over Celite and the filtrate was concentrated under reduced pressure to obtain 21.4 mg of 2,2-dimethyl-5-(5-methyl-1,3-oxazol-2-yl)-1,3-dioxan-5-amine.

후처리

  1. filtrationThe reaction mixture was filtered over Celite
  2. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-7035c7e140a449a090e10316b461e042
출처 데이터셋
uspto-grants-2016_03
특허 번호
US09278968B2

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