(1-{1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-ylcarbamoyl}-3-methylbutyl)methylcarbamic acid tert-butyl ester

Base Information

Chemical Name:(1-{1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-ylcarbamoyl}-3-methylbutyl)methylcarbamic acid tert-butyl ester
CAS No.:808749-39-5
Molecular Formula:C₃₃H₄₅F₂N₃O₄
Molecular Weight:585.735
Hs Code.:

Synonyms:(1-{1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-ylcarbamoyl}-3-methylbutyl)methylcarbamic acid tert-butyl ester

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Chemical Property of (1-{1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-ylcarbamoyl}-3-methylbutyl)methylcarbamic acid tert-butyl ester

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Technology Process of (1-{1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-ylcarbamoyl}-3-methylbutyl)methylcarbamic acid tert-butyl ester

There total 4 articles about (1-{1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-ylcarbamoyl}-3-methylbutyl)methylcarbamic 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: 40.0%

: 53363-89-6
N-t-butoxycarbonyl-N-methyl-L-leucine

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

: 808749-39-5
(1-{1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-ylcarbamoyl}-3-methylbutyl)methylcarbamic 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:

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

: 808749-39-5
(1-{1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-ylcarbamoyl}-3-methylbutyl)methylcarbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / diethyl cyanophosphonate; Et₃N / dimethylformamide / 12 h / 20 °C

2: 45 percent / Me₃SiI / CHCl₃; methanol / 6 h / 20 °C

3: 40 percent / diethyl cyanophosphonate; Et₃N / dimethylformamide / 12 h / 20 °C

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

Reference yield:

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

: 808749-39-5
(1-{1-[4,4-bis(4-fluorophenyl)butyryl]piperidin-4-ylcarbamoyl}-3-methylbutyl)methylcarbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / diethyl cyanophosphonate; Et₃N / dimethylformamide / 12 h / 20 °C

2: 45 percent / Me₃SiI / CHCl₃; methanol / 6 h / 20 °C

3: 40 percent / diethyl cyanophosphonate; Et₃N / dimethylformamide / 12 h / 20 °C

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