(R)-(3-{3-[5-(4-cyano-phenyl)-6-methoxycarbonyl-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-5,8-dihydro-[1,2,4]triazolo[4,3-a]pyrimidin-2-yl]-propane-1-sulfonyl}-propyl)-trimethylammonium chloride

Base Information

Chemical Name:(R)-(3-{3-[5-(4-cyano-phenyl)-6-methoxycarbonyl-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-5,8-dihydro-[1,2,4]triazolo[4,3-a]pyrimidin-2-yl]-propane-1-sulfonyl}-propyl)-trimethylammonium chloride
CAS No.:1426800-84-1
Molecular Formula:C₃₁H₃₆F₃N₆O₅S*Cl
Molecular Weight:697.178
Hs Code.:

(R)-(3-{3-[5-(4-cyano-phenyl)-6-methoxycarbonyl-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-5,8-dihydro-[1,2,4]triazolo[4,3-a]pyrimidin-2-yl]-propane-1-sulfonyl}-propyl)-trimethylammonium chloride

Synonyms:(R)-(3-{3-[5-(4-cyano-phenyl)-6-methoxycarbonyl-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-5,8-dihydro-[1,2,4]triazolo[4,3-a]pyrimidin-2-yl]-propane-1-sulfonyl}-propyl)-trimethylammonium chloride

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Chemical Property of (R)-(3-{3-[5-(4-cyano-phenyl)-6-methoxycarbonyl-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-5,8-dihydro-[1,2,4]triazolo[4,3-a]pyrimidin-2-yl]-propane-1-sulfonyl}-propyl)-trimethylammonium chloride

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Technology Process of (R)-(3-{3-[5-(4-cyano-phenyl)-6-methoxycarbonyl-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-5,8-dihydro-[1,2,4]triazolo[4,3-a]pyrimidin-2-yl]-propane-1-sulfonyl}-propyl)-trimethylammonium chloride

There total 12 articles about (R)-(3-{3-[5-(4-cyano-phenyl)-6-methoxycarbonyl-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-5,8-dihydro-[1,2,4]triazolo[4,3-a]pyrimidin-2-yl]-propane-1-sulfonyl}-propyl)-trimethylammonium chloride 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:

: 1426800-45-4
(R)-5-(4-cyano-phenyl)-7-methyl-3-oxo-2-{3-[3-(toluene-4-sulfonyloxy)-propane-1-sulfonyl]-propyl}-8-(3-trifluoromethyl-phenyl)-2,3,5,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidine-6-carboxylic acid methyl ester

: 75-50-3
trimethylamine

: 1426800-84-1
(R)-(3-{3-[5-(4-cyano-phenyl)-6-methoxycarbonyl-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-5,8-dihydro-[1,2,4]triazolo[4,3-a]pyrimidin-2-yl]-propane-1-sulfonyl}-propyl)-trimethylammonium chloride

Guidance literature:: (R)-5-(4-cyano-phenyl)-7-methyl-3-oxo-2-{3-[3-(toluene-4-sulfonyloxy)-propane-1-sulfonyl]-propyl}-8-(3-trifluoromethyl-phenyl)-2,3,5,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidine-6-carboxylic acid methyl ester; trimethylamine; In ethanol; at 20 ℃; for 16h;

With Amberlite IRA₄₅₈ resin;

Reference yield:

: 1426800-43-2
(R)-2-{3-[3-(tert-Butyl-dimethyl-silanyloxy)-propane-1-sulfonyl]-propyl}-5-(4-cyano-phenyl)-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-2,3,5,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidine-6-carboxylic acid methyl ester

: 1426800-84-1
(R)-(3-{3-[5-(4-cyano-phenyl)-6-methoxycarbonyl-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-5,8-dihydro-[1,2,4]triazolo[4,3-a]pyrimidin-2-yl]-propane-1-sulfonyl}-propyl)-trimethylammonium chloride

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 16 h / 20 °C

2.1: sodium hydride / tetrahydrofuran / 0.17 h / 20 °C / Inert atmosphere

2.2: 16 h

3.1: ethanol / 16 h / 20 °C

With tetrabutyl ammonium fluoride; sodium hydride; In tetrahydrofuran; ethanol;

Reference yield:

: 1426800-44-3
(R)-5-(4-cyano-phenyl)-2-[3-(3-hydroxy-propane-1-sulfonyl)-propyl]-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-2,3,5,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidine-6-carboxylic acid methyl ester

: 1426800-84-1
(R)-(3-{3-[5-(4-cyano-phenyl)-6-methoxycarbonyl-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-5,8-dihydro-[1,2,4]triazolo[4,3-a]pyrimidin-2-yl]-propane-1-sulfonyl}-propyl)-trimethylammonium chloride

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / tetrahydrofuran / 0.17 h / 20 °C / Inert atmosphere

1.2: 16 h / Inert atmosphere

2.1: ethanol / 16 h / 20 °C

2.2: Amberlite IRA₄₅₈ resin

With sodium hydride; In tetrahydrofuran; ethanol;