Hydrochloric Acid → 1-(Propan-2-yl)piperidin-4-amine dihydrochloride

HRID 491808Notes

Reaction equation

HRID 491808 reaction equation
[NH2:1][CH:2]1[CH2:7][CH2:6][N:5]([CH:8]([CH3:10])[CH3:9])[CH2:4][CH2:3]1.[ClH:11]>O1CCOCC1>[ClH:11].[ClH:11].[NH2:1][CH:2]1[CH2:7][CH2:6][N:5]([CH:8]([CH3:10])[CH3:9])[CH2:4][CH2:3]1

Participants

4

Procedure

The crude product (6.32 g) containing benzyl(1-isopropylpiperidin-4-yl)carbamate obtained in Example 382-(1) is dissolved in ethanol (100 ml), and thereto is added 10% palladium on carbon (600 mg), and the mixture is stirred at ambient temperature under hydrogen atmosphere overnight. The insoluble materials are removed by filtration, and the filtrate is concentrated under reduced pressure, and subjected to azeotropic distillation with toluene. The resulting residue is purified by NH-silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/1, then chloroform/methanol=20/1, and further 10/1) to give 4-amino-1-isopropylpiperidine (1.90 g). The resulting 4-amino-1-isopropylpiperidine is treated with 4N hydrogen chloride in dioxane to give 4-amino-1-isopropylpiperidine dihydrochloride.

Sources & evidence

ORD record
ord-ac889246e28c4b71bd4d2edbc084d6cb
Source dataset
uspto-grants-2009_05
Patent number
US07531537B2

Reaction notes

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