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Hydrochloric Acid → (3S)-N-benzyl-3-amino-2-hydroxy-5-methylhexylamine dihydrochloride

HRID 1905331
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HRID 1905331 반응식
[CH2:1]([NH:8][CH2:9][CH:10]([OH:27])[C@@H:11]([NH:16]C(OCC1C=CC=CC=1)=O)[CH2:12][CH:13]([CH3:15])[CH3:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[ClH:28]>CO.[Pd]>[ClH:28].[ClH:28].[CH2:1]([NH:8][CH2:9][CH:10]([OH:27])[C@@H:11]([NH2:16])[CH2:12][CH:13]([CH3:14])[CH3:15])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 56634722(3S)-N-benzyl-3-carbobenzoxyamino-2-hydroxy-5-methylhexylamine

생성물 1

HCID 70395546(3S)-N-benzyl-3-amino-2-hydroxy-5-methylhexylamine dihydrochloride

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of 100 mg of (3S)-3-carbobenzoxyamino-5-methyl-1,2-epoxyhexane in 10 ml of diethyl ether were added 2 g of dry silica gel and 0.1 ml of benzylamine, and the mixture was stirred for 16 hours at room temperature, then heated under reflux for 2 hours. After filtration of the silica gel, the filtrate was evaporated under reduced pressure. The residue was purified by preparative silica gel thin layer chromatography (developing solvent: lower layer of chloroform/methanol/water=8/3/1 by volume) to obtain 56 mg of (3S)-N-benzyl-3-carbobenzoxyamino-2-hydroxy-5-methylhexylamine as a colorless viscous oil. To a solution of 54 mg of the amine compound obtained in 10 ml methanol was added 0.2 ml of a 2N-hydrochloric acid. The mixture was hydrogenated over 10 mg of palladium charcoal under hydrogen atmosphere. After filtration of the catalyst, the filtrate was evaporated under reduced pressure to obtain 43 mg of (3S) -N-benzyl-3-amino-2-hydroxy-5-methylhexylamine dihydrochloride.

후처리

  1. filtrationAfter filtration of the catalyst
  2. customthe filtrate was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-dd3a7ddbf00e4e21a5be1f0ca4779e80
출처 데이터셋
uspto-grants-1989_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04841067

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