2-[2-(4-tert-butylcarbamoyl-4-cyclohexyl-piperidin-1-yl)-1-(4-fluoro-benzyl)-2-oxo-ethylcarbamoyl]-6-isopropyl-piperazine-1,4-dicarboxylic acid di-tert-butyl ester

Base Information

Chemical Name:2-[2-(4-tert-butylcarbamoyl-4-cyclohexyl-piperidin-1-yl)-1-(4-fluoro-benzyl)-2-oxo-ethylcarbamoyl]-6-isopropyl-piperazine-1,4-dicarboxylic acid di-tert-butyl ester
CAS No.:363191-99-5
Molecular Formula:C₄₃H₆₈FN₅O₇
Molecular Weight:786.041
Hs Code.:

2-[2-(4-<i>tert</i>-butylcarbamoyl-4-cyclohexyl-piperidin-1-yl)-1-(4-fluoro-benzyl)-2-oxo-ethylcarbamoyl]-6-isopropyl-piperazine-1,4-dicarboxylic acid di-<i>tert</i>-butyl ester

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Chemical Property of 2-[2-(4-tert-butylcarbamoyl-4-cyclohexyl-piperidin-1-yl)-1-(4-fluoro-benzyl)-2-oxo-ethylcarbamoyl]-6-isopropyl-piperazine-1,4-dicarboxylic acid di-tert-butyl ester

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Technology Process of 2-[2-(4-tert-butylcarbamoyl-4-cyclohexyl-piperidin-1-yl)-1-(4-fluoro-benzyl)-2-oxo-ethylcarbamoyl]-6-isopropyl-piperazine-1,4-dicarboxylic acid di-tert-butyl ester

There total 4 articles about 2-[2-(4-tert-butylcarbamoyl-4-cyclohexyl-piperidin-1-yl)-1-(4-fluoro-benzyl)-2-oxo-ethylcarbamoyl]-6-isopropyl-piperazine-1,4-dicarboxylic acid di-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: 48.0%

: 363191-98-4
N,N-Di-Boc-6-isopropyl-(S)-piperazine-2-carboxylic acid

: 363191-04-2
1-[(2R)-2-amino-3-(4-fluorophenyl)-1-oxopropyl]-4-cyclohexyl-N-(1,1-dimethylethyl)-4-piperidine carboxamide

: 363191-99-5
2-[2-(4-tert-butylcarbamoyl-4-cyclohexyl-piperidin-1-yl)-1-(4-fluoro-benzyl)-2-oxo-ethylcarbamoyl]-6-isopropyl-piperazine-1,4-dicarboxylic acid di-tert-butyl ester

Guidance literature:: With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1016/j.bmcl.2005.02.068

Reference yield:

: 363191-95-1
(S)-2-Benzyloxycarbonylamino-3-(3-methyl-2-oxo-butylamino)-propionic acid methyl ester

: 363191-99-5
2-[2-(4-tert-butylcarbamoyl-4-cyclohexyl-piperidin-1-yl)-1-(4-fluoro-benzyl)-2-oxo-ethylcarbamoyl]-6-isopropyl-piperazine-1,4-dicarboxylic acid di-tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / H₂ / Pd/C / ethanol

2: 62 percent / TEA / CH₂Cl₂

3: 53 percent / aq. NaOH / methanol

4: 48 percent / EDC; HOBt; DIEA / CH₂Cl₂

With sodium hydroxide; TEA; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; ethanol; dichloromethane;
DOI:10.1016/j.bmcl.2005.02.068

Reference yield:

: 363191-97-3
6-isopropyl-piperazine-1,2,4-tricarboxylic acid 1,4-di-tert-butyl ester 2-methyl ester

: 363191-99-5
2-[2-(4-tert-butylcarbamoyl-4-cyclohexyl-piperidin-1-yl)-1-(4-fluoro-benzyl)-2-oxo-ethylcarbamoyl]-6-isopropyl-piperazine-1,4-dicarboxylic acid di-tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 53 percent / aq. NaOH / methanol

2: 48 percent / EDC; HOBt; DIEA / CH₂Cl₂

With sodium hydroxide; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane;
DOI:10.1016/j.bmcl.2005.02.068