N-(2-(4-(4-fluorobenzylamino)-6-(4-fluorobenzylcarbamoyl)-5-hydroxypyrimidin-2-yl)propan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide

Base Information

Chemical Name:N-(2-(4-(4-fluorobenzylamino)-6-(4-fluorobenzylcarbamoyl)-5-hydroxypyrimidin-2-yl)propan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide
CAS No.:1370588-50-3
Molecular Formula:C₂₆H₂₅F₂N₇O₄
Molecular Weight:537.526
Hs Code.:

Synonyms:N-(2-(4-(4-fluorobenzylamino)-6-(4-fluorobenzylcarbamoyl)-5-hydroxypyrimidin-2-yl)propan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide

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Chemical Property of N-(2-(4-(4-fluorobenzylamino)-6-(4-fluorobenzylcarbamoyl)-5-hydroxypyrimidin-2-yl)propan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide

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Technology Process of N-(2-(4-(4-fluorobenzylamino)-6-(4-fluorobenzylcarbamoyl)-5-hydroxypyrimidin-2-yl)propan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide

There total 4 articles about N-(2-(4-(4-fluorobenzylamino)-6-(4-fluorobenzylcarbamoyl)-5-hydroxypyrimidin-2-yl)propan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide 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: 54.0%

: 1370588-47-8
methyl 5-(benzoyloxy)-6-methoxy-2-(2-(5-methyl-1,3,4-oxadiazole-2-carboxamido)propan-2-yl)pyrimidine-4-carboxylate

: 140-75-0
para-fluorobenzylamine

: 1370588-50-3
N-(2-(4-(4-fluorobenzylamino)-6-(4-fluorobenzylcarbamoyl)-5-hydroxypyrimidin-2-yl)propan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide

Guidance literature:: In methanol; for 30h; Reflux; Inert atmosphere;
DOI:10.1016/j.ejmech.2012.02.015

Reference yield:

: 857664-99-4
methyl 5-(benzoyloxy)-2-(2-(benzyloxycarbonylamino)propan-2-yl)-6-methoxypyrimidine-4-carboxylate

: 1370588-50-3
N-(2-(4-(4-fluorobenzylamino)-6-(4-fluorobenzylcarbamoyl)-5-hydroxypyrimidin-2-yl)propan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride; palladium 10% on activated carbon; hydrogen / methanol; water / 3 h / 760.05 Torr

2: triethylamine / dichloromethane; N,N-dimethyl-formamide / 2.25 h

3: methanol / 30 h / Reflux; Inert atmosphere

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; triethylamine; In methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.02.015

Reference yield:

: 1370588-46-7
2-[5-(benzoyloxy)-4-(methoxycarbonyl)-6-methoxypyrimidin-2-yl]propan-2-amine hydrochloride

: 1370588-50-3
N-(2-(4-(4-fluorobenzylamino)-6-(4-fluorobenzylcarbamoyl)-5-hydroxypyrimidin-2-yl)propan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane; N,N-dimethyl-formamide / 2.25 h

2: methanol / 30 h / Reflux; Inert atmosphere

With triethylamine; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.02.015