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2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-hydroxyethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one

Base Information Edit
  • Chemical Name:2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-hydroxyethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one
  • CAS No.:1224171-00-9
  • Molecular Formula:C22H21ClN4O4
  • Molecular Weight:440.886
  • Hs Code.:
  • Mol file:1224171-00-9.mol
2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-hydroxyethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one

Synonyms:2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-hydroxyethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one

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Chemical Property of 2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-hydroxyethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one Edit
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Technology Process of 2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-hydroxyethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one

There total 9 articles about 2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-hydroxyethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one 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:
Guidance literature:
2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-oxoethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one; With methanol; sodium tetrahydroborate; In tetrahydrofuran; at 20 ℃; for 12h;
With water; In tetrahydrofuran; methanol; at 0 - 20 ℃; pH=3; Aqueous phosphate buffer;
Guidance literature:
Multi-step reaction with 9 steps
1: potassium carbonate / acetonitrile / 14 h / 20 - 70 °C
2: N,N`-dimethylethylenediamine; copper(l) iodide; potassium carbonate / toluene / 18 h / 105 °C
3: hydrogenchloride / 1,4-dioxane / 24 h / 38 °C
4: sodium nitrite; sulfuric acid; sodium hydroxide / water; tetrahydrofuran / 0.5 h / 0 °C
5: water; tetrahydrofuran / 12 h / 20 °C
6: phosphorus pentachloride / 1,2-dimethoxyethane / 3.5 h / 0 - 20 °C
7: methyl-phenyl-thioether; trifluoroacetic acid / dichloromethane / 17 h / 20 °C
8: caesium carbonate / acetonitrile / 5 h / 80 °C
9: sodium tetrahydroborate / methanol; tetrahydrofuran / 12 h / 20 °C
With hydrogenchloride; sodium tetrahydroborate; copper(l) iodide; methyl-phenyl-thioether; phosphorus pentachloride; sulfuric acid; potassium carbonate; caesium carbonate; trifluoroacetic acid; sodium hydroxide; N,N`-dimethylethylenediamine; sodium nitrite; In tetrahydrofuran; 1,4-dioxane; methanol; 1,2-dimethoxyethane; dichloromethane; water; toluene; acetonitrile;
DOI:10.1016/j.bmcl.2015.05.008
Guidance literature:
Multi-step reaction with 6 steps
1: sodium nitrite; sulfuric acid; sodium hydroxide / water; tetrahydrofuran / 0.5 h / 0 °C
2: water; tetrahydrofuran / 12 h / 20 °C
3: phosphorus pentachloride / 1,2-dimethoxyethane / 3.5 h / 0 - 20 °C
4: methyl-phenyl-thioether; trifluoroacetic acid / dichloromethane / 17 h / 20 °C
5: caesium carbonate / acetonitrile / 5 h / 80 °C
6: sodium tetrahydroborate / methanol; tetrahydrofuran / 12 h / 20 °C
With sodium tetrahydroborate; methyl-phenyl-thioether; phosphorus pentachloride; sulfuric acid; caesium carbonate; trifluoroacetic acid; sodium hydroxide; sodium nitrite; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; dichloromethane; water; acetonitrile;
DOI:10.1016/j.bmcl.2015.05.008
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