tert-butyl [7-(1-phenethylpiperidin-4-ylamino)heptyl]carbamate

Base Information

• Chemical Name: tert-butyl [7-(1-phenethylpiperidin-4-ylamino)heptyl]carbamate
• CAS No.: 910543-86-1
• Molecular Formula: C₂₅H₄₃N₃O₂
• Molecular Weight: 417.635
• Mol file: 910543-86-1.mol

Synonyms:tert-butyl [7-(1-phenethylpiperidin-4-ylamino)heptyl]carbamate

Chemical Property of tert-butyl [7-(1-phenethylpiperidin-4-ylamino)heptyl]carbamate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of tert-butyl [7-(1-phenethylpiperidin-4-ylamino)heptyl]carbamate

There total 3 articles about tert-butyl [7-(1-phenethylpiperidin-4-ylamino)heptyl]carbamate 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: 60.0%

1-(2-phenylethyl)-4-piperidinone (39742-60-4) + N-(tert-butoxycarbonyl)-1,7-heptanediamine (99733-18-3) → tert-butyl [7-(1-phenethylpiperidin-4-ylamino)heptyl]carbamate (910543-86-1)

Guidance literature:

With 3 A molecular sieve; sodium cyanoborohydride; acetic acid; In methanol; pH=6 - 7;

DOI:10.1016/j.bmc.2006.06.007

Reference yield:

heptane-1,7-diamine (646-19-5) → tert-butyl [7-(1-phenethylpiperidin-4-ylamino)heptyl]carbamate (910543-86-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 99 percent / CHCl₃ / 0 - 20 °C

2: 60 percent / NaBH₃CN; molecular sieves 3 Angstroem; AcOH / methanol / pH 6 - 7

With 3 A molecular sieve; sodium cyanoborohydride; acetic acid; In methanol; chloroform;

DOI:10.1016/j.bmc.2006.06.007

Reference yield:

di-tert-butyl dicarbonate (24424-99-5) → tert-butyl [7-(1-phenethylpiperidin-4-ylamino)heptyl]carbamate (910543-86-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 99 percent / CHCl₃ / 0 - 20 °C

2: 60 percent / NaBH₃CN; molecular sieves 3 Angstroem; AcOH / methanol / pH 6 - 7

With 3 A molecular sieve; sodium cyanoborohydride; acetic acid; In methanol; chloroform;

DOI:10.1016/j.bmc.2006.06.007

upstream raw materials:

1-(2-phenylethyl)-4-piperidinone

N-(tert-butoxycarbonyl)-1,7-heptanediamine

heptane-1,7-diamine

di-tert-butyl dicarbonate

Downstream raw materials:

N-[7-(N²,N³-bis(tert-butoxycarbonyl)guanidino)heptyl]-N-(1-phenethylpiperidin-4-yl)propanamide

tert-butyl {7-[(1-phenethylpiperidin-4-yl)propionylamino]heptyl}carbamate