HCID 21949207, compound → 1-(3-Amino-propyl)-piperidin-4-ol

HRID 2215561Notes

Reaction equation

HRID 2215561 reaction equation
[OH:1][CH:2]1[CH2:7][CH2:6][N:5]([CH2:8][CH2:9][CH2:10][NH:11]C(=O)OCC2C=CC=CC=2)[CH2:4][CH2:3]1>[C].[Pd].C(O)C>[NH2:11][CH2:10][CH2:9][CH2:8][N:5]1[CH2:4][CH2:3][CH:2]([OH:1])[CH2:7][CH2:6]1

Participants

4

Procedure

Ethanol (200 ml) and palladium carbon (2.5 g) were added to benzyl N-(3-(4-hydroxypiperidino)propyl)carbamate (2.96 g); and the reaction mixture was stirred vigorously under hydrogen atmosphere overnight. Palladium carbon was removed by filtration, and the filtrate was concentrated to yield the title compound (1.5 g).

Workup

  1. customPalladium carbon was removed by filtration
  2. concentrationthe filtrate was concentrated

Sources & evidence

ORD record
ord-3b4820da3e76444ca754f3af246c8ff3
Source dataset
uspto-grants-2006_09
Patent number
US07109219B2

Reaction notes

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