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N-tert-butyl-1-benzhydryl-3-methylazetidin-3-amine hydrochloride → HCID 68455629, 화합물

HRID 474000
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HRID 474000 반응식
[ClH:1].[C:2]([NH:6][C:7]1([CH3:24])[CH2:10][N:9](C(C2C=CC=CC=2)C2C=CC=CC=2)[CH2:8]1)([CH3:5])([CH3:4])[CH3:3]>C(O)C.[OH-].[OH-].[Pd+2]>[ClH:1].[C:2]([NH:6][C:7]1([CH3:24])[CH2:10][NH:9][CH2:8]1)([CH3:5])([CH3:4])[CH3:3]
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참가 물질

4

반응물 1

HCID 68457650N-tert-butyl-1-benzhydryl-3-methylazetidin-3-amine hydrochloride

생성물 1

HCID 68455629HCID 68455629, 화합물

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 702Ethanol용매

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온도
40 °C

실험 절차

To a slurry of N-tert-butyl-1-benzhydryl-3-methylazetidin-3-amine hydrochloride (1.69 g, 4.91 mmol) in ethanol (30 ml) was added 10% Palladium hydroxide on carbon (160 mg) and the mixture degassed three times with nitrogen and three times with hydrogen. The mixture was then stirred under a hydrogen atmosphere 40° C. (warm water bath) for 3 h and then at room temperature for a further 12 h. The reaction was degassed with nitrogen and filtered through celite and concentrated. The compound was used crude in subsequent chemistry. 1H NMR (MeOH) 1.50 (9H, s), 1.99 (3H, s), 4.19 (2H, d), 4.91 (2H, d).

후처리

  1. customthe mixture degassed three times with nitrogen and three times with hydrogen
  2. temperature(warm water bath) for 3 h
  3. customThe reaction was degassed with nitrogen
  4. filtrationfiltered through celite
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-0782814961ff4b6a99953b6ac4568a52
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637511B2

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