Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

1-(TETRAHYDRO-2H-PYRAN-4-YL)PIPERIDIN-4-AMINE synthesis

2synthesis methods
873537-63-4 Synthesis
tert-butyl 1-(tetrahydro-2H-pyran-4-yl)piperidin-4-ylcarbamate

873537-63-4
9 suppliers
inquiry

-

Yield:794471-13-9 92%

Reaction Conditions:

Stage #1: tert-butyl (1-(tetrahydro-2H-pyran-4-yl)piperidin-4-yl)carbamatewith hydrogenchloride in 1,4-dioxane;methanol at 20;
Stage #2: with sodium hydroxide in dichloromethane;water;

Steps:

9.b

9.2 g (0.0323 mol, 1 eq) of 1 ,1-dimethylethyl [1-(tetrahydro-2/7-pyran-4-yl)-4- piperidinyl]carbamate, 65 mL (0.258 mol, 8 eq) of 4 M HCI in dioxane, and enough methanol to achieve dissolution were combined and stirred at ambient temperature overnight. The reaction mixture was then evaporated. Dichloromethane and 1 M NaOH were added. Sodium chloride was then added to saturate the aqueous layer. The aqueous layer was extracted with dichloromethane twice. The organic layers were combined, dried with sodium sulfate, and evaporated to yield 5.5 g (92% yield) of 1- (tetrahydro-2/-/-pyran-4-yl)-4-piperidinamine as a low melting white solid. 1H-NMR (400 MHz, DMSO-Qf6): δ 3.86 (m, 2H), 3.24 (m, 2H), 2.77 (m, 2H), 2.46 (m, 1H), 2.35 (m, 1 H), EPO 2.25-1.05 (v br s, 2H, NH2), 2.07 (m, 2H), 1.64 (m, 4H), 1.39 (m, 2H), 1.16 (m, 2H); MS (ESI): 185 [M+H]+.

References:

WO2007/36711,2007,A1 Location in patent:Page/Page column 44-45