4-nitrobenzyl(1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[7-(4-nitrobenzyloxy-carbonylamino)acetylimidazo[5,1-b]thiazol-2-yl]-1-carbapen-2-em-3-carboxylate

Base Information

Chemical Name:4-nitrobenzyl(1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[7-(4-nitrobenzyloxy-carbonylamino)acetylimidazo[5,1-b]thiazol-2-yl]-1-carbapen-2-em-3-carboxylate
CAS No.:258840-63-0
Molecular Formula:C₃₂H₂₈N₆O₁₁S
Molecular Weight:704.674
Hs Code.:

4-nitrobenzyl(1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[7-(4-nitrobenzyloxy-carbonylamino)acetylimidazo[5,1-b]thiazol-2-yl]-1-carbapen-2-em-3-carboxylate

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Chemical Property of 4-nitrobenzyl(1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[7-(4-nitrobenzyloxy-carbonylamino)acetylimidazo[5,1-b]thiazol-2-yl]-1-carbapen-2-em-3-carboxylate

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Technology Process of 4-nitrobenzyl(1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[7-(4-nitrobenzyloxy-carbonylamino)acetylimidazo[5,1-b]thiazol-2-yl]-1-carbapen-2-em-3-carboxylate

There total 7 articles about 4-nitrobenzyl(1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[7-(4-nitrobenzyloxy-carbonylamino)acetylimidazo[5,1-b]thiazol-2-yl]-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:

: 4457-32-3
4-nitrobenzyl chloroformate

: 258840-63-0
4-nitrobenzyl(1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[7-(4-nitrobenzyloxy-carbonylamino)acetylimidazo[5,1-b]thiazol-2-yl]-1-carbapen-2-em-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide / tetrahydrofuran; water; ethyl acetate

With sodium hydroxide; In tetrahydrofuran; water; ethyl acetate;

Reference yield:

: 251-89-8
imidazo[5,1-b]thiazole

: 258840-63-0
4-nitrobenzyl(1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[7-(4-nitrobenzyloxy-carbonylamino)acetylimidazo[5,1-b]thiazol-2-yl]-1-carbapen-2-em-3-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

2: N-Bromosuccinimide; chloro-trimethyl-silane / tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; ethyl acetate; N,N-dimethyl-formamide

3: hydrogenchloride; sodium hydroxide / Pd-C / tetrahydrofuran; water

4: tetrahydrofuran; ethyl acetate

With hydrogenchloride; sodium hydroxide; N-Bromosuccinimide; chloro-trimethyl-silane; Pd-C; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; water; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 258838-72-1
7-acetylimidazo[5,1-b]thiazole

: 258840-63-0
4-nitrobenzyl(1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[7-(4-nitrobenzyloxy-carbonylamino)acetylimidazo[5,1-b]thiazol-2-yl]-1-carbapen-2-em-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide; chloro-trimethyl-silane / tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; ethyl acetate; N,N-dimethyl-formamide

2: hydrogenchloride; sodium hydroxide / Pd-C / tetrahydrofuran; water

3: tetrahydrofuran; ethyl acetate

With hydrogenchloride; sodium hydroxide; N-Bromosuccinimide; chloro-trimethyl-silane; Pd-C; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; water; ethyl acetate; N,N-dimethyl-formamide;