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5-Thiazolecarboxylic acid, 2-[1-[2,6-dichloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)phenyl] -1-methylethyl]-4-phenyl-, 1,1-dimethylethyl ester

Base Information
  • Chemical Name:5-Thiazolecarboxylic acid, 2-[1-[2,6-dichloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)phenyl] -1-methylethyl]-4-phenyl-, 1,1-dimethylethyl ester
  • CAS No.:325968-64-7
  • Molecular Formula:C26H24Cl2N4O4S
  • Molecular Weight:559.473
  • Hs Code.:
5-Thiazolecarboxylic acid,
2-[1-[2,6-dichloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)phenyl]
-1-methylethyl]-4-phenyl-, 1,1-dimethylethyl ester

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Chemical Property of 5-Thiazolecarboxylic acid, 2-[1-[2,6-dichloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)phenyl] -1-methylethyl]-4-phenyl-, 1,1-dimethylethyl ester
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SDS file from LookChem

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Technology Process of 5-Thiazolecarboxylic acid, 2-[1-[2,6-dichloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)phenyl] -1-methylethyl]-4-phenyl-, 1,1-dimethylethyl ester

There total 8 articles about 5-Thiazolecarboxylic acid, 2-[1-[2,6-dichloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)phenyl] -1-methylethyl]-4-phenyl-, 1,1-dimethylethyl ester 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:
2,6-dichloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-α,α-dimethylbenzeneethane-thioamide; 1,1-dimethylethyl α-bromo-β-oxo-benzenepropionate; With potassium carbonate; In acetonitrile; at 20 ℃;
In tert-butyl alcohol; Heating;
DOI:10.1021/jm049479m
Guidance literature:
Multi-step reaction with 7 steps
1.1: 15.0 g / H2 / Raney Ni / methanol / 1 h / 20 °C / 2250.18 Torr
2.1: aq. HCl; AcOH; NaNO2 / 1.83 h / 10 °C
2.2: 84 percent / aq. NaOAc / 0.67 h
3.1: KOAc; AcOH / 3 h / 120 °C
4.1: 100.6 g / aq. HCl / 4 h / Heating
5.1: 44 percent / thioglycolic acid / 4 h / 100 °C
6.1: 40 percent / diisopropylethylamine; H2S; pyridine / 24 h / 80 °C
7.1: K2CO3 / acetonitrile / 20 °C
7.2: 50 percent / 2-methyl-propan-2-ol / Heating
With pyridine; hydrogenchloride; hydrogen sulfide; hydrogen; potassium acetate; potassium carbonate; acetic acid; mercaptoacetic acid; N-ethyl-N,N-diisopropylamine; sodium nitrite; nickel; In methanol; acetonitrile;
DOI:10.1021/jm049479m
Guidance literature:
Multi-step reaction with 2 steps
1.1: 40 percent / diisopropylethylamine; H2S; pyridine / 24 h / 80 °C
2.1: K2CO3 / acetonitrile / 20 °C
2.2: 50 percent / 2-methyl-propan-2-ol / Heating
With pyridine; hydrogen sulfide; potassium carbonate; N-ethyl-N,N-diisopropylamine; In acetonitrile;
DOI:10.1021/jm049479m
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