4-(4-fluorobenzylcarbamoyl)-6-methoxy-2-(2-(5-methyl-1,3,4-oxadiazole-2-carboxamido)propan-2-yl)pyrimidin-5-yl benzoate

Base Information

Chemical Name:4-(4-fluorobenzylcarbamoyl)-6-methoxy-2-(2-(5-methyl-1,3,4-oxadiazole-2-carboxamido)propan-2-yl)pyrimidin-5-yl benzoate
CAS No.:1370588-56-9
Molecular Formula:C₂₇H₂₅FN₆O₆
Molecular Weight:548.531
Hs Code.:

Synonyms:4-(4-fluorobenzylcarbamoyl)-6-methoxy-2-(2-(5-methyl-1,3,4-oxadiazole-2-carboxamido)propan-2-yl)pyrimidin-5-yl benzoate

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Chemical Property of 4-(4-fluorobenzylcarbamoyl)-6-methoxy-2-(2-(5-methyl-1,3,4-oxadiazole-2-carboxamido)propan-2-yl)pyrimidin-5-yl benzoate

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Technology Process of 4-(4-fluorobenzylcarbamoyl)-6-methoxy-2-(2-(5-methyl-1,3,4-oxadiazole-2-carboxamido)propan-2-yl)pyrimidin-5-yl benzoate

There total 5 articles about 4-(4-fluorobenzylcarbamoyl)-6-methoxy-2-(2-(5-methyl-1,3,4-oxadiazole-2-carboxamido)propan-2-yl)pyrimidin-5-yl benzoate 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: 85.0%

: 1370588-48-9
N-(2-(4-(4-fluorobenzylcarbamoyl)-5-hydroxy-6-methoxypyrimidin-2-yl)propan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide

: 98-88-4
benzoyl chloride

: 1370588-56-9
4-(4-fluorobenzylcarbamoyl)-6-methoxy-2-(2-(5-methyl-1,3,4-oxadiazole-2-carboxamido)propan-2-yl)pyrimidin-5-yl benzoate

Guidance literature:: With triethylamine; In dichloromethane; for 3h; Reflux;
DOI:10.1016/j.ejmech.2012.02.015

Reference yield:

: methyl 2-(2(((benzyloxy)carbonyl)amino)propan-2-yl)-5,6-dihydroxy-1,6-dihydropyrimidine-4-carboxylate

: 1370588-56-9
4-(4-fluorobenzylcarbamoyl)-6-methoxy-2-(2-(5-methyl-1,3,4-oxadiazole-2-carboxamido)propan-2-yl)pyrimidin-5-yl benzoate

Guidance literature:: Multi-step reaction with 6 steps

1.1: pyridine / 10 h / 20 °C

2.1: lithium hydride / 1,4-dioxane / 1 h / 40 °C

2.2: 3 h / 60 °C

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

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

5.1: methanol / 20 h / Reflux; Inert atmosphere

5.3: 0 °C / pH 2

6.1: triethylamine / dichloromethane / 3 h / Reflux

With pyridine; hydrogenchloride; palladium 10% on activated carbon; hydrogen; lithium hydride; triethylamine; In 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide;
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

: 1370588-56-9
4-(4-fluorobenzylcarbamoyl)-6-methoxy-2-(2-(5-methyl-1,3,4-oxadiazole-2-carboxamido)propan-2-yl)pyrimidin-5-yl benzoate

Guidance literature:: Multi-step reaction with 4 steps

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

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

3.1: methanol / 20 h / Reflux; Inert atmosphere

3.3: 0 °C / pH 2

4.1: triethylamine / dichloromethane / 3 h / Reflux

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