5-({[(3-hydroxypropyl)amino]carbonyl}amino)-3-(4-nitrophenyl)isothiazol-4-carboxamide

Base Information

Chemical Name:5-({[(3-hydroxypropyl)amino]carbonyl}amino)-3-(4-nitrophenyl)isothiazol-4-carboxamide
CAS No.:1446246-92-9
Molecular Formula:C₁₄H₁₅N₅O₅S
Molecular Weight:365.37
Hs Code.:

Synonyms:5-({[(3-hydroxypropyl)amino]carbonyl}amino)-3-(4-nitrophenyl)isothiazol-4-carboxamide

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Chemical Property of 5-({[(3-hydroxypropyl)amino]carbonyl}amino)-3-(4-nitrophenyl)isothiazol-4-carboxamide

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Technology Process of 5-({[(3-hydroxypropyl)amino]carbonyl}amino)-3-(4-nitrophenyl)isothiazol-4-carboxamide

There total 8 articles about 5-({[(3-hydroxypropyl)amino]carbonyl}amino)-3-(4-nitrophenyl)isothiazol-4-carboxamide 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%

: 1446246-91-8
methyl 3-[({[4-(aminocarbonyl)-3-(4-nitrophenyl)isothiazol-5-yl]amino}carbonyl)amino]propanoate

: 1446246-92-9
5-({[(3-hydroxypropyl)amino]carbonyl}amino)-3-(4-nitrophenyl)isothiazol-4-carboxamide

Guidance literature:: methyl 3-[({[4-(aminocarbonyl)-3-(4-nitrophenyl)isothiazol-5-yl]amino}carbonyl)amino]propanoate; With sodium tetrahydroborate; In tetrahydrofuran; Reflux;

With methanol; sodium tetrahydroborate; In tetrahydrofuran; for 2h; Reflux;

Reference yield:

: 605661-26-5
2-[amino(4-nitrophenyl)methylene]malononitrile

: 1446246-92-9
5-({[(3-hydroxypropyl)amino]carbonyl}amino)-3-(4-nitrophenyl)isothiazol-4-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: O,O-Diethyl hydrogen phosphorodithioate / ethanol; water / 100 °C / Inert atmosphere

2.1: dihydrogen peroxide / ethanol / 22 h / Inert atmosphere

3.1: potassium carbonate / tetrahydrofuran; dimethyl sulfoxide / 0.25 h / 20 °C

3.2: 20 °C

4.1: sulfuric acid / 1.83 h / 45 °C

4.2: Cooling with ice

5.1: sodium tetrahydroborate / tetrahydrofuran / Reflux

5.2: 2 h / Reflux

With sodium tetrahydroborate; sulfuric acid; dihydrogen peroxide; potassium carbonate; O,O-Diethyl hydrogen phosphorodithioate; In tetrahydrofuran; ethanol; water; dimethyl sulfoxide;

Reference yield:

: 909028-96-2
3-amino-3-(4-nitrophenyl)-2-thioformamidoacrylonitrile

: 1446246-92-9
5-({[(3-hydroxypropyl)amino]carbonyl}amino)-3-(4-nitrophenyl)isothiazol-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: dihydrogen peroxide / ethanol / 22 h / Inert atmosphere

2.1: potassium carbonate / tetrahydrofuran; dimethyl sulfoxide / 0.25 h / 20 °C

2.2: 20 °C

3.1: sulfuric acid / 1.83 h / 45 °C

3.2: Cooling with ice

4.1: sodium tetrahydroborate / tetrahydrofuran / Reflux

4.2: 2 h / Reflux

With sodium tetrahydroborate; sulfuric acid; dihydrogen peroxide; potassium carbonate; In tetrahydrofuran; ethanol; dimethyl sulfoxide;