Technology Process of 3-cyano-N-{5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5dihydroisoxazol-3-yl]-2-methylthiophen-3-ylmethyl}propionamide
There total 7 articles about 3-cyano-N-{5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5dihydroisoxazol-3-yl]-2-methylthiophen-3-ylmethyl}propionamide 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:
-
With
benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine;
In
dichloromethane;
at 20 ℃;
for 4h;
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: sodium acetate; bromine / water / 12 h / 20 °C
2.1: lithium hydride / tetrahydrofuran / 5 h / 60 °C / Inert atmosphere
3.1: triethylamine; trifluoroacetic anhydride / 12 h / 0 - 20 °C
4.1: hydroxylamine hydrochloride; sodium hydroxide / ethanol / 12 h / 20 °C
5.1: tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 1 h / 120 °C / Microwave irradiation
6.1: dimethylsulfide borane complex / tetrahydrofuran / 0.5 h / Reflux
6.2: 0.5 h / Reflux
7.1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / dichloromethane / 4 h / 20 °C
With
dimethylsulfide borane complex; hydroxylamine hydrochloride; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; bromine; sodium acetate; lithium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic anhydride; sodium hydroxide;
tetrakis(triphenylphosphine) palladium(0);
In
tetrahydrofuran; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: lithium hydride / tetrahydrofuran / 5 h / 60 °C / Inert atmosphere
2.1: triethylamine; trifluoroacetic anhydride / 12 h / 0 - 20 °C
3.1: hydroxylamine hydrochloride; sodium hydroxide / ethanol / 12 h / 20 °C
4.1: tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 1 h / 120 °C / Microwave irradiation
5.1: dimethylsulfide borane complex / tetrahydrofuran / 0.5 h / Reflux
5.2: 0.5 h / Reflux
6.1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / dichloromethane / 4 h / 20 °C
With
dimethylsulfide borane complex; hydroxylamine hydrochloride; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; lithium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic anhydride; sodium hydroxide;
tetrakis(triphenylphosphine) palladium(0);
In
tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;