Methanol → [1-(2-Phenylethylsulfonyl)piperidin-4-yl]methanamine

HRID 1827177Notes

Reaction equation

HRID 1827177 reaction equation
C(OC(=O)[NH:10][CH2:11][CH:12]1[CH2:17][CH2:16][N:15]([S:18]([CH:21]=[CH:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)(=[O:20])=[O:19])[CH2:14][CH2:13]1)C1C=CC=CC=1.CO.[H][H]>[OH-].[Pd+2].[OH-].O1CCCC1>[C:23]1([CH2:22][CH2:21][S:18]([N:15]2[CH2:14][CH2:13][CH:12]([CH2:11][NH2:10])[CH2:17][CH2:16]2)(=[O:19])=[O:20])[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1

Participants

6

Reactant 3

HCID 887MethanolHCID 69413281HCID 69413281, compoundHCID 178418361HCID 178418361, compound

Product 1

HCID 22135729[1-(2-Phenylethylsulfonyl)piperidin-4-yl]methanamine

Reagents, catalysts & solvents 2

HCID 9942167Palladium hydroxideCatalystHCID 8028TetrahydrofuranSolvent

Procedure

A mixture of [1-(2-phenyl-ethenesulfonyl)-piperidin-4-ylmethyl]-carbamic acid benzyl ester (2.5 g), 20% palladium hydroxide (1 g) on carbon, 200 mL of methanol and 50 mL of tetrahydrofuran were shaken under 50 psi of hydrogen for 2 days at room temperature. The catalyst was filtered off and washed with 250 mL of methanol. Concentration under reduced pressure gave C-[1-(2-phenyl-ethanesulfonyl)-piperidin-4-yl]-methylamine as white solid.

Workup

  1. filtrationThe catalyst was filtered off
  2. washwashed with 250 mL of methanol
  3. concentrationConcentration under reduced pressure

Sources & evidence

ORD record
ord-f646d21afd2246cd85d6d255ecf9d37d
Source dataset
uspto-grants-2006_05
Patent number
US07053089B2

Reaction notes

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