(2R,5S,6R)-6-((S)-1-Hydroxy-ethyl)-7-oxo-3-[(Z)-phenylimino]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester

Base Information

Chemical Name:(2R,5S,6R)-6-((S)-1-Hydroxy-ethyl)-7-oxo-3-[(Z)-phenylimino]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester
CAS No.:113396-95-5
Molecular Formula:C₂₁H₁₉N₃O₆S
Molecular Weight:441.464
Hs Code.:

Synonyms:(2R,5S,6R)-6-((S)-1-Hydroxy-ethyl)-7-oxo-3-[(Z)-phenylimino]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester

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Chemical Property of (2R,5S,6R)-6-((S)-1-Hydroxy-ethyl)-7-oxo-3-[(Z)-phenylimino]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester

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Technology Process of (2R,5S,6R)-6-((S)-1-Hydroxy-ethyl)-7-oxo-3-[(Z)-phenylimino]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester

There total 5 articles about (2R,5S,6R)-6-((S)-1-Hydroxy-ethyl)-7-oxo-3-[(Z)-phenylimino]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl 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: 15.0%

: 113396-93-3
(Z)-3-Acetylsulfanyl-2-[(2R,3R)-2-chloro-3-((S)-1-hydroxy-ethyl)-4-oxo-azetidin-1-yl]-3-phenylamino-acrylic acid 4-nitro-benzyl ester

: 113396-95-5
(2R,5S,6R)-6-((S)-1-Hydroxy-ethyl)-7-oxo-3-[(Z)-phenylimino]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester

: 113396-94-4
(5R,6S)-6-((R)-1-Hydroxy-ethyl)-7-oxo-3-phenylamino-4-thia-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl ester

Guidance literature:: With 1H-imidazole; In 1,4-dioxane; water;
DOI:10.1016/S0040-4039(00)96102-1

Reference yield:

: 85768-12-3
{(2S,3R)-3-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-ethylsulfanyl-4-oxo-azetidin-1-yl}-acetic acid 4-nitro-benzyl ester

: 113396-95-5
(2R,5S,6R)-6-((S)-1-Hydroxy-ethyl)-7-oxo-3-[(Z)-phenylimino]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: lithium hexamethyldisilazide

2: 5M aq. HCl / tetrahydrofuran / 20 °C

3: Cl₂ / CCl₄; CHCl₃ / 0 °C

4: 15 percent / imidazole / H₂O; dioxane

With 1H-imidazole; hydrogenchloride; chlorine; lithium hexamethyldisilazane; In tetrahydrofuran; 1,4-dioxane; tetrachloromethane; chloroform; water;
DOI:10.1016/S0040-4039(00)96102-1

Reference yield:

: (Z)-3-Acetylsulfanyl-2-[(2R,3S)-2-ethylsulfanyl-3-((R)-1-hydroxy-ethyl)-4-oxo-azetidin-1-yl]-3-phenylamino-acrylic acid 4-nitro-benzyl ester

: 113396-95-5
(2R,5S,6R)-6-((S)-1-Hydroxy-ethyl)-7-oxo-3-[(Z)-phenylimino]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Cl₂ / CCl₄; CHCl₃ / 0 °C

2: 15 percent / imidazole / H₂O; dioxane

With 1H-imidazole; chlorine; In 1,4-dioxane; tetrachloromethane; chloroform; water;
DOI:10.1016/S0040-4039(00)96102-1