5-(azetidin-3-yl)-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole hydrochloride

Base Information

Chemical Name:5-(azetidin-3-yl)-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole hydrochloride
CAS No.:1426135-80-9
Molecular Formula:C₁₂H₁₂N₄O₃*ClH
Molecular Weight:296.713
Hs Code.:

Synonyms:5-(azetidin-3-yl)-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole hydrochloride

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Chemical Property of 5-(azetidin-3-yl)-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole hydrochloride

Chemical Property:

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Technology Process of 5-(azetidin-3-yl)-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole hydrochloride

There total 3 articles about 5-(azetidin-3-yl)-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole hydrochloride 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:

: 1426135-79-6
tert-butyl 3-(3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazol-5-yl)azetidine-1-carboxylate

: 1426135-80-9
5-(azetidin-3-yl)-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole hydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; acetonitrile; at 20 ℃; for 1h;

Reference yield:

: 1426671-13-7,74229-76-8
N'-hydroxy-4-methyl-3-nitrobenzimidamide

: 1426135-80-9
5-(azetidin-3-yl)-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 1,1'-carbonyldiimidazole / 1-methyl-pyrrolidin-2-one / 0.2 h / 115 °C / Microwave irradiation

2: hydrogenchloride / acetonitrile; 1,4-dioxane / 1 h / 20 °C

With hydrogenchloride; 1,1'-carbonyldiimidazole; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; acetonitrile;

Reference yield:

: 939-79-7
4-cyano-2-nitrotoluene

: 1426135-80-9
5-(azetidin-3-yl)-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine; hydroxylamine hydrochloride / ethanol / 3 h / 78 °C

2: 1,1'-carbonyldiimidazole / 1-methyl-pyrrolidin-2-one / 0.2 h / 115 °C / Microwave irradiation

3: hydrogenchloride / acetonitrile; 1,4-dioxane / 1 h / 20 °C

With hydrogenchloride; hydroxylamine hydrochloride; N-ethyl-N,N-diisopropylamine; 1,1'-carbonyldiimidazole; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; ethanol; acetonitrile;