[3-(1-phenethyl-piperidin-4-ylamino)-propyl]-carbamic acid benzyl ester

Base Information

Chemical Name:[3-(1-phenethyl-piperidin-4-ylamino)-propyl]-carbamic acid benzyl ester
CAS No.:439099-17-9
Molecular Formula:C₂₄H₃₃N₃O₂
Molecular Weight:395.545
Hs Code.:

Synonyms:[3-(1-phenethyl-piperidin-4-ylamino)-propyl]-carbamic acid benzyl ester

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Chemical Property of [3-(1-phenethyl-piperidin-4-ylamino)-propyl]-carbamic acid benzyl ester

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Technology Process of [3-(1-phenethyl-piperidin-4-ylamino)-propyl]-carbamic acid benzyl ester

There total 1 articles about [3-(1-phenethyl-piperidin-4-ylamino)-propyl]-carbamic acid benzyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 45.0%

: 39742-60-4
1-(2-phenylethyl)-4-piperidinone

: 46460-73-5
N-benzyloxycarbonyl-1,3-diaminopropane

: 439099-17-9
[3-(1-phenethyl-piperidin-4-ylamino)-propyl]-carbamic acid benzyl ester

Guidance literature:: With hydrogenchloride; 3 A molecular sieve; sodium cyanoborohydride; In methanol; at 20 ℃; for 24h; pH=6;
DOI:10.1016/S0968-0896(01)00356-X

Reference yield:

: 439099-17-9
[3-(1-phenethyl-piperidin-4-ylamino)-propyl]-carbamic acid benzyl ester

: 439099-19-1
N-(3-amino-propyl)-N-(1-phenethyl-piperidin-4-yl)-propionamide

Guidance literature:: Multi-step reaction with 2 steps

1: 72 percent / 3 h / Heating

2: 98 percent / H₂ / Pd/C / acetic acid; methanol / 6 h / 1810.02 - 2068.59 Torr

With hydrogen; palladium on activated charcoal; In methanol; acetic acid;
DOI:10.1016/S0968-0896(01)00356-X

Reference yield:

: 439099-17-9
[3-(1-phenethyl-piperidin-4-ylamino)-propyl]-carbamic acid benzyl ester

: 439099-20-4
C₃₀H₄₉N₅O₅

Guidance literature:: Multi-step reaction with 3 steps

1: 72 percent / 3 h / Heating

2: 98 percent / H₂ / Pd/C / acetic acid; methanol / 6 h / 1810.02 - 2068.59 Torr

3: 51 percent / TEA; HgCl₂ / CH₂Cl₂ / 25 h / 0 - 20 °C

With TEA; hydrogen; mercury dichloride; palladium on activated charcoal; In methanol; dichloromethane; acetic acid;
DOI:10.1016/S0968-0896(01)00356-X