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CyclohexanaMine, 4-[4-(cyclopropylMethyl)-1-piperazinyl]-, trans- synthesis

10synthesis methods
Benzenemethanamine, N-[trans-4-[4-(cyclopropylmethyl)-1-piperazinyl]cyclohexyl]-N-(phenylmethyl)-

755039-89-5
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CyclohexanaMine, 4-[4-(cyclopropylMethyl)-1-piperazinyl]-, trans-

876461-31-3
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Yield:876461-31-3 100%

Reaction Conditions:

with hydrogen;acetic acid;palladium 10% on activated carbon in methanol at 20 - 30; under 2280.15 Torr; for 12 h;

Steps:

16.2

Step 2 (trans)-4-[4-(Cyclopropylmethyl)piperazin-1-yl]cyclohexanamine; (trans)-N,N-Dibenzyl-4-[4-(cyclopropylmethyl)piperazin-1-yl]cyclohexanamine 16a (1.41 g, 3.38 mmol) was dissolved in 15 mL of methanol followed by the addition of palladium / carbon (706 mg, 10%) and 0.1 mL of acetic acid, filled with hydrogen three times. The reaction mixture was reacted for 12 hours at 3 atomosphere of hydrogen, added with 3 g alkaline aluminum oxide (200-300 mesh) and filtered. The filtrate was concentrated under reduced pressure to obtain the title compound (trans)-4-[4-(cyclopropylmethyl)piperazin-1-yl]cyclohexanamine 16b (900 mg, yield: 100%) as a colorless solid. MS m/z (ESI): 238.2 [M+1]

References:

EP2481739,2012,A1 Location in patent:Page/Page column 48

882660-40-4 Synthesis
N-((1r,4r)-4-(4-(cyclopropylMethyl)piperazin-1-yl)cyclohexyl)acetaMide

882660-40-4
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CyclohexanaMine, 4-[4-(cyclopropylMethyl)-1-piperazinyl]-, trans-

876461-31-3
18 suppliers
inquiry