p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-2-[[N-(4-hydroxymethylbenzyl)-N-methyl]aminothiocarbonylthio]-1-methyl-1-carbapen-2-em-3-carboxylate

Base Information

Chemical Name:p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-2-[[N-(4-hydroxymethylbenzyl)-N-methyl]aminothiocarbonylthio]-1-methyl-1-carbapen-2-em-3-carboxylate
CAS No.:268541-94-2
Molecular Formula:C₂₇H₂₉N₃O₇S₂
Molecular Weight:571.675
Hs Code.:

p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-2-[[N-(4-hydroxymethylbenzyl)-N-methyl]aminothiocarbonylthio]-1-methyl-1-carbapen-2-em-3-carboxylate

Synonyms:p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-2-[[N-(4-hydroxymethylbenzyl)-N-methyl]aminothiocarbonylthio]-1-methyl-1-carbapen-2-em-3-carboxylate

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Chemical Property of p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-2-[[N-(4-hydroxymethylbenzyl)-N-methyl]aminothiocarbonylthio]-1-methyl-1-carbapen-2-em-3-carboxylate

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Technology Process of p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-2-[[N-(4-hydroxymethylbenzyl)-N-methyl]aminothiocarbonylthio]-1-methyl-1-carbapen-2-em-3-carboxylate

There total 1 articles about p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-2-[[N-(4-hydroxymethylbenzyl)-N-methyl]aminothiocarbonylthio]-1-methyl-1-carbapen-2-em-3-carboxylate 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: 42.0%

: 93711-81-0,90776-59-3,189188-38-3
(4-nitrophenyl)methyl (4R,5R,6S)-3-[(diphenoxyphosphinyl)oxy]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate

: (4-hydroxymethyl-benzyl)-methyl-dithiocarbamic acid

: 268541-94-2
p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-2-[[N-(4-hydroxymethylbenzyl)-N-methyl]aminothiocarbonylthio]-1-methyl-1-carbapen-2-em-3-carboxylate

Guidance literature:: With lithium chloride; In tetrahydrofuran; at 20 ℃;
DOI:10.1016/S0968-0896(01)00044-X

Reference yield:

: 10147-36-1
n-propanesulfonyl chloride

: 268541-94-2
p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-2-[[N-(4-hydroxymethylbenzyl)-N-methyl]aminothiocarbonylthio]-1-methyl-1-carbapen-2-em-3-carboxylate

: (4R,5S,6S)-6-((R)-1-Hydroxy-ethyl)-4-methyl-3-{methyl-[4-(propane-1-sulfonyloxymethyl)-benzyl]-thiocarbamoylsulfanyl}-7-oxo-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl ester

Guidance literature:: With diisopropylamine; In tetrahydrofuran; at 0 ℃; for 2h;
DOI:10.1016/S0968-0896(01)00044-X

Reference yield:

: 268541-94-2
p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-2-[[N-(4-hydroxymethylbenzyl)-N-methyl]aminothiocarbonylthio]-1-methyl-1-carbapen-2-em-3-carboxylate

: 365217-13-6
(4R,5S,6S)-6-((R)-1-Hydroxy-ethyl)-3-[(4-iodomethyl-benzyl)-methyl-thiocarbamoylsulfanyl]-4-methyl-7-oxo-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: diisopropylamine / tetrahydrofuran / 2 h / 0 °C

2: NaI / acetone / 2 h / 20 °C

With diisopropylamine; sodium iodide; In tetrahydrofuran; acetone;
DOI:10.1016/S0968-0896(01)00044-X