(1-(4-chloro-benzyl)-2-oxo-2-{4-[1-(phenylacetylamino-methyl)-cyclohexyl]-piperazin-1-yl}-ethyl)-carbamic acid tert-butyl ester

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Chemical Name:(1-(4-chloro-benzyl)-2-oxo-2-{4-[1-(phenylacetylamino-methyl)-cyclohexyl]-piperazin-1-yl}-ethyl)-carbamic acid tert-butyl ester
CAS No.:511540-39-9
Molecular Formula:C₃₃H₄₅ClN₄O₄
Molecular Weight:597.198
Hs Code.:

(1-(4-chloro-benzyl)-2-oxo-2-{4-[1-(phenylacetylamino-methyl)-cyclohexyl]-piperazin-1-yl}-ethyl)-carbamic acid <i>tert</i>-butyl ester

Synonyms:(1-(4-chloro-benzyl)-2-oxo-2-{4-[1-(phenylacetylamino-methyl)-cyclohexyl]-piperazin-1-yl}-ethyl)-carbamic acid tert-butyl ester

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Chemical Property of (1-(4-chloro-benzyl)-2-oxo-2-{4-[1-(phenylacetylamino-methyl)-cyclohexyl]-piperazin-1-yl}-ethyl)-carbamic acid tert-butyl ester

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Technology Process of (1-(4-chloro-benzyl)-2-oxo-2-{4-[1-(phenylacetylamino-methyl)-cyclohexyl]-piperazin-1-yl}-ethyl)-carbamic acid tert-butyl ester

There total 4 articles about (1-(4-chloro-benzyl)-2-oxo-2-{4-[1-(phenylacetylamino-methyl)-cyclohexyl]-piperazin-1-yl}-ethyl)-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: 93.0%

: 511540-38-8
2-phenyl-N-(1-piperazin-1-yl-cyclohexylmethyl)-acetamide

: 57292-44-1
N-Boc-D-(4-Cl)Phe-OH

: 511540-39-9
(1-(4-chloro-benzyl)-2-oxo-2-{4-[1-(phenylacetylamino-methyl)-cyclohexyl]-piperazin-1-yl}-ethyl)-carbamic acid tert-butyl ester

Guidance literature:: With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane; at 20 ℃; for 16h;
DOI:10.1016/j.bmcl.2005.08.061

Reference yield:

: 139754-93-1
1-(4-benzylpiperazin-1-yl)cyclohexanecarbonitrile

: 511540-39-9
(1-(4-chloro-benzyl)-2-oxo-2-{4-[1-(phenylacetylamino-methyl)-cyclohexyl]-piperazin-1-yl}-ethyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: LiAlH₄ / diethyl ether / 0.5 h / 20 °C

2: Et₃N / CH₂Cl₂ / 0 - 20 °C

3: 100 percent / HCO₂NH₄ / Pd-C / methanol / 0.67 h / Heating

4: 93 percent / EDC; HOBT / CH₂Cl₂ / 16 h / 20 °C

With lithium aluminium tetrahydride; ammonium formate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; palladium on activated charcoal; In methanol; diethyl ether; dichloromethane;
DOI:10.1016/j.bmcl.2005.08.061

Reference yield:

: 511538-96-8
(1-(4-benzylpiperazin-1-yl)cyclohexyl)methanamine

: 511540-39-9
(1-(4-chloro-benzyl)-2-oxo-2-{4-[1-(phenylacetylamino-methyl)-cyclohexyl]-piperazin-1-yl}-ethyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: Et₃N / CH₂Cl₂ / 0 - 20 °C

2: 100 percent / HCO₂NH₄ / Pd-C / methanol / 0.67 h / Heating

3: 93 percent / EDC; HOBT / CH₂Cl₂ / 16 h / 20 °C

With ammonium formate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1016/j.bmcl.2005.08.061