HCID 18426153, compound → HCID 18426178, compound

HRID 2187801Notes

Reaction equation

HRID 2187801 reaction equation
[Cl:1][C:2]1[CH:22]=[CH:21][C:5]([CH2:6][N:7]2[CH2:12][CH2:11][CH2:10][CH:9]([NH:13]C(OC(C)(C)C)=O)[CH2:8]2)=[CH:4][CH:3]=1>Cl.CCOCC>[ClH:1].[ClH:1].[NH2:13][CH:9]1[CH2:10][CH2:11][CH2:12][N:7]([CH2:6][C:5]2[CH:4]=[CH:3][C:2]([Cl:1])=[CH:22][CH:21]=2)[CH2:8]1

Participants

3

Reactant 1

HCID 18426153HCID 18426153, compound

Product 1

HCID 18426178HCID 18426178, compound

Reagents, catalysts & solvents 1

HCID 10953452Ether hydrochlorideSolvent

Conditions

Temperature
25 °C

Procedure

A solution of 1-(4-chlorobenzyl)-3-{(tert-butoxycarbonyl)amino}piperidine (2.55 g, 7.85 mmol) in CH2OH (25 mL) was treated with 1 N HCl-Et2O (50 mL). The reaction mixture was stirred at 25° C. for 15 h. The solvent was removed under reduced pressure to afford 3-amino-l-(4-chlorobenzyl)piperidine dihydrochloride as an amorphous solid (2.49 g, quant).

Workup

  1. customThe solvent was removed under reduced pressure

Sources & evidence

ORD record
ord-ff46a6a0b6cb40239d13e8f3d116d9a8
Source dataset
uspto-grants-2002_06
Patent number
US06410566B1

Reaction notes

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