1-Benzyl-4-(N-Boc-amino)piperidine → 4-(N-Boc-amino)piperidine

HRID 19463ノート

反応式

HRID 19463 の反応式
C([N:8]1[CH2:13][CH2:12][CH:11]([NH:14][C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:10][CH2:9]1)C1C=CC=CC=1.[H][H]>CO.[Pd]>[C:18]([O:17][C:15]([NH:14][CH:11]1[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]1)=[O:16])([CH3:21])([CH3:19])[CH3:20]

参加物

5

反応物 2

HCID 44386181-Benzyl-4-(N-Boc-amino)piperidineHCID 178418361HCID 178418361、化合物

生成物 1

HCID 7238334-(N-Boc-amino)piperidine収率 91%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

A solution of 1-benzyl-4-tertbutyloxycarbonylaminopiperidine 5 (7.95 g; 27.4 mmol) in 120 ml of MeOH is poured into a hydrogenation reactor. 10% Pd/c-based catalyst is added (1.46 g; 1.38 mmol) and the mixture is subjected to a hydrogen pressure of 3.5 bars (50 psi) for 24 hours in a Parr type shaker. After filtration on celite and washing with methanol, the medium is concentrated in order to produce 4.98 g (Yield=91%) of product in the form of white crystals.

後処理

  1. filtrationAfter filtration on celite
  2. washwashing with methanol
  3. concentrationthe medium is concentrated in order

出典と根拠

ORDレコード
ord-7fbbc4b12374417a9e72e3284df826eb
出典データセット
uspto-grants-2010_06
特許番号
US07745413B2

反応ノート

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