(1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-yl)carbamic acid tert-butyl ester

Base Information

Chemical Name:(1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-yl)carbamic acid tert-butyl ester
CAS No.:808749-33-9
Molecular Formula:C₂₆H₃₂F₂N₂O₃
Molecular Weight:458.548
Hs Code.:

Synonyms:(1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-yl)carbamic acid tert-butyl ester

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Chemical Property of (1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-yl)carbamic acid tert-butyl ester

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Technology Process of (1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-yl)carbamic acid tert-butyl ester

There total 1 articles about (1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-yl)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: 98.0%

: 20662-52-6
4,4-bis(4-fluorophenyl)butanoic acid

: 73874-95-0
(piperidin-4-yl)carbamic acid tert-butyl ester

: 808749-33-9
(1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-yl)carbamic acid tert-butyl ester

Guidance literature:: With diethyl cyanophosphonate; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 12h;
DOI:10.1021/jm049923l

Reference yield: 45.0%

: 808749-33-9
(1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-yl)carbamic acid tert-butyl ester

: 808749-34-0
1-(4-aminopiperidin-1-yl)-4,4-bis(4-fluorophenyl)butan-1-one

Guidance literature:: With trimethylsilyl iodide; In methanol; chloroform; at 20 ℃; for 6h;
DOI:10.1021/jm049923l

Reference yield:

: 808749-33-9
(1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-yl)carbamic acid tert-butyl ester

: 2-amino-4-methylpentanoic acid {1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-yl}amide

Guidance literature:: Multi-step reaction with 3 steps

1: 45 percent / Me₃SiI / CHCl₃; methanol / 6 h / 20 °C

2: 70 percent / diethyl cyanophosphonate; Et₃N / dimethylformamide / 12 h / 20 °C

3: 69 percent / aq. HCl / ethyl acetate / 24 h / 20 °C

With hydrogenchloride; trimethylsilyl iodide; diethyl cyanophosphonate; triethylamine; In methanol; chloroform; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm049923l