p-nitrobenzyl 3-<(2-azidoethyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate

Base Information

Chemical Name:p-nitrobenzyl 3-<(2-azidoethyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate
CAS No.:75527-02-5
Molecular Formula:C₁₅H₁₃N₅O₅S₂
Molecular Weight:407.431
Hs Code.:

Synonyms:p-nitrobenzyl 3-<(2-azidoethyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate

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Chemical Property of p-nitrobenzyl 3-<(2-azidoethyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate

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Technology Process of p-nitrobenzyl 3-<(2-azidoethyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate

There total 6 articles about p-nitrobenzyl 3-<(2-azidoethyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-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: 80.0%

: 75527-01-4
p-nitrobenzyl 3-<(2-hydroxyethyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate

: 75527-02-5
p-nitrobenzyl 3-<(2-azidoethyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate

Guidance literature:: With hydrogen azide; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; benzene; for 0.25h; Ambient temperature;

Reference yield:

: 77597-10-5
4-<<<<2-<(tetrahydropyran-2-yl)oxy>ethyl>thio>thiocarbonyl>thio>-2-azetidinone

: 75527-02-5
p-nitrobenzyl 3-<(2-azidoethyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: 83 percent / benzene / 9 h / Heating

2: 1.) 2,6-lutidine, thionyl chloride; 2.) 2,6-lutidine / 1.) THF, -10 deg C, 30 min; 2.) THF, -10 deg C, then 50 deg C, 11 h

3: 5 percent / xylene / 23 h / 125 °C

4: 80 percent / triphenylphosphine, 0.7 M hydrogen azide sol., diethylazodicarboxylate / tetrahydrofuran; benzene / 0.25 h / Ambient temperature

With 2,6-dimethylpyridine; hydrogen azide; thionyl chloride; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; xylene; benzene;

Reference yield:

: 77597-12-7
Hydroxy-{2-oxo-4-[2-(tetrahydro-pyran-2-yloxy)-ethylsulfanylthiocarbonylsulfanyl]-azetidin-1-yl}-acetic acid 4-nitro-benzyl ester

: 75527-02-5
p-nitrobenzyl 3-<(2-azidoethyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) 2,6-lutidine, thionyl chloride; 2.) 2,6-lutidine / 1.) THF, -10 deg C, 30 min; 2.) THF, -10 deg C, then 50 deg C, 11 h

2: 5 percent / xylene / 23 h / 125 °C

3: 80 percent / triphenylphosphine, 0.7 M hydrogen azide sol., diethylazodicarboxylate / tetrahydrofuran; benzene / 0.25 h / Ambient temperature

With 2,6-dimethylpyridine; hydrogen azide; thionyl chloride; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; xylene; benzene;