(2R,6R,7R)-7-tert-Butoxycarbonylamino-8-oxo-3-[2-oxo-1-phenyl-piperidin-(3E)-ylidenemethyl]-5-thia-1-aza-bicyclo[4.2.0]oct-3-ene-2-carboxylic acid benzhydryl ester

Base Information

Chemical Name:(2R,6R,7R)-7-tert-Butoxycarbonylamino-8-oxo-3-[2-oxo-1-phenyl-piperidin-(3E)-ylidenemethyl]-5-thia-1-aza-bicyclo[4.2.0]oct-3-ene-2-carboxylic acid benzhydryl ester
CAS No.:161754-81-0
Molecular Formula:C₃₇H₃₇N₃O₆S
Molecular Weight:651.783
Hs Code.:

(2R,6R,7R)-7-tert-Butoxycarbonylamino-8-oxo-3-[2-oxo-1-phenyl-piperidin-(3E)-ylidenemethyl]-5-thia-1-aza-bicyclo[4.2.0]oct-3-ene-2-carboxylic acid benzhydryl ester

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Chemical Property of (2R,6R,7R)-7-tert-Butoxycarbonylamino-8-oxo-3-[2-oxo-1-phenyl-piperidin-(3E)-ylidenemethyl]-5-thia-1-aza-bicyclo[4.2.0]oct-3-ene-2-carboxylic acid benzhydryl ester

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Technology Process of (2R,6R,7R)-7-tert-Butoxycarbonylamino-8-oxo-3-[2-oxo-1-phenyl-piperidin-(3E)-ylidenemethyl]-5-thia-1-aza-bicyclo[4.2.0]oct-3-ene-2-carboxylic acid benzhydryl ester

There total 4 articles about (2R,6R,7R)-7-tert-Butoxycarbonylamino-8-oxo-3-[2-oxo-1-phenyl-piperidin-(3E)-ylidenemethyl]-5-thia-1-aza-bicyclo[4.2.0]oct-3-ene-2-carboxylic acid benzhydryl 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:

: 41339-29-1
2,5-Dibromo-pentanoyl chloride

: 161754-81-0
(2R,6R,7R)-7-tert-Butoxycarbonylamino-8-oxo-3-[2-oxo-1-phenyl-piperidin-(3E)-ylidenemethyl]-5-thia-1-aza-bicyclo[4.2.0]oct-3-ene-2-carboxylic acid benzhydryl ester

Guidance literature:: Multi-step reaction with 3 steps

1: Et₃N / CH₂Cl₂

2: Dowex 2x 10, 50percent aq. NaOH / CH₂Cl₂ / Ambient temperature

3: 1.) PPh₃ / 1.) benzene, reflux, 2.) 1,2-dichloroethane, 1,2-epoxybutane, reflux

With sodium hydroxide; Dowex 2x 10; triethylamine; triphenylphosphine; In dichloromethane;
DOI:10.1021/jm950886v

Reference yield:

: 77868-78-1
2,5-Dibromo-pentanoic acid phenylamide

: 161754-81-0
(2R,6R,7R)-7-tert-Butoxycarbonylamino-8-oxo-3-[2-oxo-1-phenyl-piperidin-(3E)-ylidenemethyl]-5-thia-1-aza-bicyclo[4.2.0]oct-3-ene-2-carboxylic acid benzhydryl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Dowex 2x 10, 50percent aq. NaOH / CH₂Cl₂ / Ambient temperature

2: 1.) PPh₃ / 1.) benzene, reflux, 2.) 1,2-dichloroethane, 1,2-epoxybutane, reflux

With sodium hydroxide; Dowex 2x 10; triphenylphosphine; In dichloromethane;
DOI:10.1021/jm950886v

Reference yield:

: 62-53-3
aniline

: 161754-81-0
(2R,6R,7R)-7-tert-Butoxycarbonylamino-8-oxo-3-[2-oxo-1-phenyl-piperidin-(3E)-ylidenemethyl]-5-thia-1-aza-bicyclo[4.2.0]oct-3-ene-2-carboxylic acid benzhydryl ester

Guidance literature:: Multi-step reaction with 3 steps

1: Et₃N / CH₂Cl₂

2: Dowex 2x 10, 50percent aq. NaOH / CH₂Cl₂ / Ambient temperature

3: 1.) PPh₃ / 1.) benzene, reflux, 2.) 1,2-dichloroethane, 1,2-epoxybutane, reflux

With sodium hydroxide; Dowex 2x 10; triethylamine; triphenylphosphine; In dichloromethane;
DOI:10.1021/jm950886v