{3-[3-(4-trifluoromethyl-benzyl)-piperidin-1-yl]-propyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{3-[3-(4-trifluoromethyl-benzyl)-piperidin-1-yl]-propyl}-carbamic acid tert-butyl ester
CAS No.:745817-72-5
Molecular Formula:C₂₁H₃₁F₃N₂O₂
Molecular Weight:400.485
Hs Code.:

{3-[3-(4-trifluoromethyl-benzyl)-piperidin-1-yl]-propyl}-carbamic acid <i>tert</i>-butyl ester

Synonyms:{3-[3-(4-trifluoromethyl-benzyl)-piperidin-1-yl]-propyl}-carbamic acid tert-butyl ester

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Chemical Property of {3-[3-(4-trifluoromethyl-benzyl)-piperidin-1-yl]-propyl}-carbamic acid tert-butyl ester

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Technology Process of {3-[3-(4-trifluoromethyl-benzyl)-piperidin-1-yl]-propyl}-carbamic acid tert-butyl ester

There total 7 articles about {3-[3-(4-trifluoromethyl-benzyl)-piperidin-1-yl]-propyl}-carbamic acid tert-butyl 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: 80.0%

: 58885-60-2
N-(tert-butoxycarbonyl)-3-aminopropanal

: 3-(4-trifluoromethyl-benzyl)-piperidine; hydrochloride

: 745817-72-5
{3-[3-(4-trifluoromethyl-benzyl)-piperidin-1-yl]-propyl}-carbamic acid tert-butyl ester

Guidance literature:: With sodium tris(acetoxy)borohydride; In 1,2-dichloro-ethane; for 14h;
DOI:10.1016/j.bmcl.2004.01.059

Reference yield:

: 58885-58-8
N-tert-butoxycarbonyl-3-aminopropanol

: 745817-72-5
{3-[3-(4-trifluoromethyl-benzyl)-piperidin-1-yl]-propyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: tetrapropylammonium perruthenate; NMO; 4A molecular sieves / CH₂Cl₂; acetonitrile / 1 h

2: 80 percent / NaBH(OAc)3 / 1,2-dichloro-ethane / 14 h

With N-methyl-2-indolinone; tetrapropylammonium perruthennate; 4 A molecular sieve; sodium tris(acetoxy)borohydride; In dichloromethane; 1,2-dichloro-ethane; acetonitrile;
DOI:10.1016/j.bmcl.2004.01.059

Reference yield:

: 85275-45-2
N-tert-butoxycarbonyl-3-piperidinol

: 745817-72-5
{3-[3-(4-trifluoromethyl-benzyl)-piperidin-1-yl]-propyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: tetrapropylammonium perruthenate; NMO; 4A molecular sieves / CH₂Cl₂; acetonitrile / 1 h

2: n-BuLi / tetrahydrofuran / -78 °C

3: 100 percent / H₂ / Pd/C / methanol / 12 h / 2068.59 Torr

4: 100 percent / HCl / dioxane / 3 h

5: 80 percent / NaBH(OAc)3 / 1,2-dichloro-ethane / 14 h

With hydrogenchloride; n-butyllithium; N-methyl-2-indolinone; tetrapropylammonium perruthennate; 4 A molecular sieve; hydrogen; sodium tris(acetoxy)borohydride; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; 1,2-dichloro-ethane; acetonitrile; 2: Wittig reaction;
DOI:10.1016/j.bmcl.2004.01.059