ethyl 1-(2-nitrophenyl)-5-((1S,2S,3S)-1,2,3-trihydroxy butyl)-1H-1,2,3-triazole-4-carboxylate

Base Information

Chemical Name:ethyl 1-(2-nitrophenyl)-5-((1S,2S,3S)-1,2,3-trihydroxy butyl)-1H-1,2,3-triazole-4-carboxylate
CAS No.:1573124-23-8
Molecular Formula:C₁₅H₁₈N₄O₇
Molecular Weight:366.331
Hs Code.:

Synonyms:ethyl 1-(2-nitrophenyl)-5-((1S,2S,3S)-1,2,3-trihydroxy butyl)-1H-1,2,3-triazole-4-carboxylate

Suppliers and Price of ethyl 1-(2-nitrophenyl)-5-((1S,2S,3S)-1,2,3-trihydroxy butyl)-1H-1,2,3-triazole-4-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of ethyl 1-(2-nitrophenyl)-5-((1S,2S,3S)-1,2,3-trihydroxy butyl)-1H-1,2,3-triazole-4-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl 1-(2-nitrophenyl)-5-((1S,2S,3S)-1,2,3-trihydroxy butyl)-1H-1,2,3-triazole-4-carboxylate

There total 5 articles about ethyl 1-(2-nitrophenyl)-5-((1S,2S,3S)-1,2,3-trihydroxy butyl)-1H-1,2,3-triazole-4-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%

: 1573124-08-9
ethyl 5-((4S,5S)-5-((S)-1-hydroxyethyl)-2,2-dimethyl-1,3-dioxolan-4-yl)-1-(2-nitrophenyl)-1H-1,2,3-triazole-4-carboxylate

: 1573124-23-8
ethyl 1-(2-nitrophenyl)-5-((1S,2S,3S)-1,2,3-trihydroxy butyl)-1H-1,2,3-triazole-4-carboxylate

Guidance literature:: With trifluoroacetic acid; In dichloromethane; water; at 0 - 20 ℃; for 2h;
DOI:10.1016/j.bmcl.2014.01.077

Reference yield:

: 4159-66-4
(S)-1-((4S,5S)-5-((S)-1-hydroxyethyl)-2,2-dimethyl-1,3-dioxolan-4-yl)ethane-1,2-diol

: 1573124-23-8
ethyl 1-(2-nitrophenyl)-5-((1S,2S,3S)-1,2,3-trihydroxy butyl)-1H-1,2,3-triazole-4-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium periodate / methanol; water / 1.5 h / 20 °C

2: tin(II) chloride dihdyrate / dichloromethane / 7 h / 0 - 20 °C

3: pyrrolidine / dimethyl sulfoxide / 14 h / 60 °C

4: trifluoroacetic acid / water; dichloromethane / 2 h / 0 - 20 °C

With pyrrolidine; sodium periodate; tin(II) chloride dihdyrate; trifluoroacetic acid; In methanol; dichloromethane; water; dimethyl sulfoxide; 3: |Huisgen Cycloaddition;
DOI:10.1016/j.bmcl.2014.01.077

Reference yield:

: 3969-60-6
(R)-1-((4S,4'S,5S)-2,2,2',2'-tetramethyl-4,4'-bi(1,3-dioxolan)-5-yl)ethanol

: 1573124-23-8
ethyl 1-(2-nitrophenyl)-5-((1S,2S,3S)-1,2,3-trihydroxy butyl)-1H-1,2,3-triazole-4-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: acetic acid / water / 20 °C

2: sodium periodate / methanol; water / 1.5 h / 20 °C

3: tin(II) chloride dihdyrate / dichloromethane / 7 h / 0 - 20 °C

4: pyrrolidine / dimethyl sulfoxide / 14 h / 60 °C

5: trifluoroacetic acid / water; dichloromethane / 2 h / 0 - 20 °C

With pyrrolidine; sodium periodate; tin(II) chloride dihdyrate; acetic acid; trifluoroacetic acid; In methanol; dichloromethane; water; dimethyl sulfoxide; 4: |Huisgen Cycloaddition;
DOI:10.1016/j.bmcl.2014.01.077