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(Z)-5-cyclopropyl-2-(4-fluorophenyl)-N-hydroxy-6-(N'-isopentylmethylsulfonamido)benzofuran-3-carboximidamide

Base Information Edit
  • Chemical Name:(Z)-5-cyclopropyl-2-(4-fluorophenyl)-N-hydroxy-6-(N'-isopentylmethylsulfonamido)benzofuran-3-carboximidamide
  • CAS No.:1383851-68-0
  • Molecular Formula:C24H28FN3O4S
  • Molecular Weight:473.568
  • Hs Code.:
  • Mol file:1383851-68-0.mol
(Z)-5-cyclopropyl-2-(4-fluorophenyl)-N-hydroxy-6-(N'-isopentylmethylsulfonamido)benzofuran-3-carboximidamide

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Chemical Property of (Z)-5-cyclopropyl-2-(4-fluorophenyl)-N-hydroxy-6-(N'-isopentylmethylsulfonamido)benzofuran-3-carboximidamide Edit
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Technology Process of (Z)-5-cyclopropyl-2-(4-fluorophenyl)-N-hydroxy-6-(N'-isopentylmethylsulfonamido)benzofuran-3-carboximidamide

There total 12 articles about (Z)-5-cyclopropyl-2-(4-fluorophenyl)-N-hydroxy-6-(N'-isopentylmethylsulfonamido)benzofuran-3-carboximidamide 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:
Multi-step reaction with 15 steps
1.1: potassium tert-butylate / toluene / 78 °C / Inert atmosphere
1.2: 78 °C / Inert atmosphere
1.3: 78 °C / Inert atmosphere
2.1: zinc(II) chloride / tetrahydrofuran; toluene / 6 h / Reflux; Inert atmosphere
3.1: 1-methyl-pyrrolidin-2-one; caesium carbonate / 4 h / 50 °C / Inert atmosphere
4.1: nitric acid / chloroform / 1 h / 0 - 20 °C
5.1: boron trichloride / dichloromethane / 1 h / 0 - 20 °C
5.2: 20 °C
6.1: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h
7.1: potassium fluoride dihydrate; sodium bromide / tetrakis(triphenylphosphine) palladium(0) / toluene / 18 h / 125 °C / Inert atmosphere; sealed vessel
8.1: iron; ammonium chloride / tetrahydrofuran; ethanol; water / 1.5 h / Inert atmosphere; Reflux
9.1: pyridine / dichloromethane / 3.33 h / 20 °C / Inert atmosphere
10.1: potassium carbonate / dimethyl sulfoxide / 3 h / Inert atmosphere
11.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h
11.2: 0.33 h
12.1: dipyridinium dichromate / dichloromethane / 3 h
13.1: hydroxylamine hydrochloride; sodium carbonate / ethanol; water / 2.5 h / Reflux
14.1: acetic anhydride / 16 h / 135 °C
15.1: hydroxylamine / ethanol; water / 0.5 h / 140 °C / microwave tube; sealed tube
With pyridine; 1-methyl-pyrrolidin-2-one; dmap; lithium aluminium tetrahydride; dipyridinium dichromate; potassium fluoride dihydrate; hydroxylamine hydrochloride; potassium tert-butylate; hydroxylamine; nitric acid; acetic anhydride; boron trichloride; iron; sodium carbonate; potassium carbonate; ammonium chloride; caesium carbonate; N-ethyl-N,N-diisopropylamine; sodium bromide; zinc(II) chloride; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; ethanol; dichloromethane; chloroform; water; dimethyl sulfoxide; toluene;
Guidance literature:
Multi-step reaction with 14 steps
1.1: zinc(II) chloride / tetrahydrofuran; toluene / 6 h / Reflux; Inert atmosphere
2.1: 1-methyl-pyrrolidin-2-one; caesium carbonate / 4 h / 50 °C / Inert atmosphere
3.1: nitric acid / chloroform / 1 h / 0 - 20 °C
4.1: boron trichloride / dichloromethane / 1 h / 0 - 20 °C
4.2: 20 °C
5.1: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h
6.1: potassium fluoride dihydrate; sodium bromide / tetrakis(triphenylphosphine) palladium(0) / toluene / 18 h / 125 °C / Inert atmosphere; sealed vessel
7.1: iron; ammonium chloride / tetrahydrofuran; ethanol; water / 1.5 h / Inert atmosphere; Reflux
8.1: pyridine / dichloromethane / 3.33 h / 20 °C / Inert atmosphere
9.1: potassium carbonate / dimethyl sulfoxide / 3 h / Inert atmosphere
10.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h
10.2: 0.33 h
11.1: dipyridinium dichromate / dichloromethane / 3 h
12.1: hydroxylamine hydrochloride; sodium carbonate / ethanol; water / 2.5 h / Reflux
13.1: acetic anhydride / 16 h / 135 °C
14.1: hydroxylamine / ethanol; water / 0.5 h / 140 °C / microwave tube; sealed tube
With pyridine; 1-methyl-pyrrolidin-2-one; dmap; lithium aluminium tetrahydride; dipyridinium dichromate; potassium fluoride dihydrate; hydroxylamine hydrochloride; hydroxylamine; nitric acid; acetic anhydride; boron trichloride; iron; sodium carbonate; potassium carbonate; ammonium chloride; caesium carbonate; N-ethyl-N,N-diisopropylamine; sodium bromide; zinc(II) chloride; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; ethanol; dichloromethane; chloroform; water; dimethyl sulfoxide; toluene;
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