4-(2,3-Dichlorophenyl)-3-(ethoxycarbonyl)-2-<<2-<(4-hydroxythiazol-2-yl)amino>ethoxy>methyl>-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine

Base Information

Chemical Name:4-(2,3-Dichlorophenyl)-3-(ethoxycarbonyl)-2-<<2-<(4-hydroxythiazol-2-yl)amino>ethoxy>methyl>-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine
CAS No.:118070-88-5
Molecular Formula:C₂₃H₂₅Cl₂N₃O₆S
Molecular Weight:542.44
Hs Code.:

4-(2,3-Dichlorophenyl)-3-(ethoxycarbonyl)-2-<<2-<(4-hydroxythiazol-2-yl)amino>ethoxy>methyl>-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine

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Chemical Property of 4-(2,3-Dichlorophenyl)-3-(ethoxycarbonyl)-2-<<2-<(4-hydroxythiazol-2-yl)amino>ethoxy>methyl>-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine

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Technology Process of 4-(2,3-Dichlorophenyl)-3-(ethoxycarbonyl)-2-<<2-<(4-hydroxythiazol-2-yl)amino>ethoxy>methyl>-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine

There total 3 articles about 4-(2,3-Dichlorophenyl)-3-(ethoxycarbonyl)-2-<<2-<(4-hydroxythiazol-2-yl)amino>ethoxy>methyl>-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine 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:

: 88150-50-9
2-[(2-aminoethoxy)methyl]-4-(2,3-dichlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine

: 118070-88-5
4-(2,3-Dichlorophenyl)-3-(ethoxycarbonyl)-2-<<2-<(4-hydroxythiazol-2-yl)amino>ethoxy>methyl>-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / CaCO₃ / CH₂Cl₂; H₂O / 18 h / Ambient temperature

2: 74 percent / ethanolic NH₃ / 2.5 h / Heating

3: 1.) triethylamine / 1.) CH₂Cl₂, 0 deg C, 1 h, then r.t., 18 h, then 40 deg C, 2 h, 2.) toluene, reflux, 5 h

With ammonia; triethylamine; calcium carbonate; In dichloromethane; water;
DOI:10.1021/jm00123a009

Reference yield:

: 118070-95-4
4-(2,3-Dichlorophenyl)-3-(ethoxycarbonyl)-2-<<2-(isothiocyano)ethoxy>methyl>-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine

: 118070-88-5
4-(2,3-Dichlorophenyl)-3-(ethoxycarbonyl)-2-<<2-<(4-hydroxythiazol-2-yl)amino>ethoxy>methyl>-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / ethanolic NH₃ / 2.5 h / Heating

2: 1.) triethylamine / 1.) CH₂Cl₂, 0 deg C, 1 h, then r.t., 18 h, then 40 deg C, 2 h, 2.) toluene, reflux, 5 h

With ammonia; triethylamine;
DOI:10.1021/jm00123a009

Reference yield:

: 105-36-2
ethyl bromoacetate

: 93848-92-1
4-(2,3-Dichlorophenyl)-3-(ethoxycarbonyl)-5-(methoxycarbonyl)-6-methyl-2-<<2-(thioureido)ethoxy>methyl>-1,4-dihydropyridine

: 118070-88-5
4-(2,3-Dichlorophenyl)-3-(ethoxycarbonyl)-2-<<2-<(4-hydroxythiazol-2-yl)amino>ethoxy>methyl>-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridine

Guidance literature:: With triethylamine; Yield given. Multistep reaction; 1.) CH₂Cl₂, 0 deg C, 1 h, then r.t., 18 h, then 40 deg C, 2 h, 2.) toluene, reflux, 5 h;
DOI:10.1021/jm00123a009