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

HRID 1905331
ノート
印刷プレビュー

反応式

HRID 1905331 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

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.

後処理

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

出典と根拠

ORDレコード
ord-dd3a7ddbf00e4e21a5be1f0ca4779e80
出典データセット
uspto-grants-1989_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04841067

反応ノート

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