[1-{[1-(5-tert-butyl-[1,3,4]oxadiazole-2-carbonyl)-2-methyl-propylcarbamoyl]-methyl}-2-(4-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester

Base Information

Chemical Name:[1-{[1-(5-tert-butyl-[1,3,4]oxadiazole-2-carbonyl)-2-methyl-propylcarbamoyl]-methyl}-2-(4-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester
CAS No.:208847-82-9
Molecular Formula:C₃₁H₃₃FN₆O₆
Molecular Weight:604.638
Hs Code.:

[1-{[1-(5-<i>tert</i>-butyl-[1,3,4]oxadiazole-2-carbonyl)-2-methyl-propylcarbamoyl]-methyl}-2-(4-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester

Synonyms:[1-{[1-(5-tert-butyl-[1,3,4]oxadiazole-2-carbonyl)-2-methyl-propylcarbamoyl]-methyl}-2-(4-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester

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Chemical Property of [1-{[1-(5-tert-butyl-[1,3,4]oxadiazole-2-carbonyl)-2-methyl-propylcarbamoyl]-methyl}-2-(4-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester

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Technology Process of [1-{[1-(5-tert-butyl-[1,3,4]oxadiazole-2-carbonyl)-2-methyl-propylcarbamoyl]-methyl}-2-(4-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester

There total 6 articles about [1-{[1-(5-tert-butyl-[1,3,4]oxadiazole-2-carbonyl)-2-methyl-propylcarbamoyl]-methyl}-2-(4-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl 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:

Reference yield:

: 208847-72-7
[1-({1-[(5-tert-butyl-[1,3,4]oxadiazol-2-yl)-hydroxy-methyl]-2-methyl-propylcarbamoyl}-methyl)-2-(4-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester

: 208847-82-9
[1-{[1-(5-tert-butyl-[1,3,4]oxadiazole-2-carbonyl)-2-methyl-propylcarbamoyl]-methyl}-2-(4-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester

Guidance literature:: With oxalyl dichloride; dimethyl sulfoxide; In dichloromethane; at -70 ℃; for 2h;
DOI:10.1021/jm000410y

Reference yield:

: 598-98-1
Methyl pivalate

: 208847-82-9
[1-{[1-(5-tert-butyl-[1,3,4]oxadiazole-2-carbonyl)-2-methyl-propylcarbamoyl]-methyl}-2-(4-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: 60 percent / hydrazine hydrate / 28 h / Heating

2.1: 69 percent / p-toluenesulfonic acid monohydrate / 80 - 120 °C

3.1: n-BuLi; MgBr₂*OEt₂ / hexane / 1.5 h / -70 - -45 °C

3.2: 53 percent / hexane; tetrahydrofuran / -45 - -20 °C

4.1: 100 percent / HCl / dioxane / 2 h / 20 °C

5.1: HOBt*H₂O; EDC*HCl; N-methylmorpholine / dimethylformamide / 3.5 h / 20 °C

6.1: oxalyl chloride; DMSO / CH₂Cl₂ / 2 h / -70 °C

With 4-methyl-morpholine; hydrogenchloride; n-butyllithium; oxalyl dichloride; benzotriazol-1-ol; toluene-4-sulfonic acid; hydrazine hydrate; dimethyl sulfoxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; magnesium bromide; In 1,4-dioxane; hexane; dichloromethane; N,N-dimethyl-formamide; 6.1: Swern oxidation;
DOI:10.1021/jm000410y

Reference yield:

: 42826-42-6
pivalohydrazide

: 208847-82-9
[1-{[1-(5-tert-butyl-[1,3,4]oxadiazole-2-carbonyl)-2-methyl-propylcarbamoyl]-methyl}-2-(4-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 69 percent / p-toluenesulfonic acid monohydrate / 80 - 120 °C

2.1: n-BuLi; MgBr₂*OEt₂ / hexane / 1.5 h / -70 - -45 °C

2.2: 53 percent / hexane; tetrahydrofuran / -45 - -20 °C

3.1: 100 percent / HCl / dioxane / 2 h / 20 °C

4.1: HOBt*H₂O; EDC*HCl; N-methylmorpholine / dimethylformamide / 3.5 h / 20 °C

5.1: oxalyl chloride; DMSO / CH₂Cl₂ / 2 h / -70 °C

With 4-methyl-morpholine; hydrogenchloride; n-butyllithium; oxalyl dichloride; benzotriazol-1-ol; toluene-4-sulfonic acid; dimethyl sulfoxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; magnesium bromide; In 1,4-dioxane; hexane; dichloromethane; N,N-dimethyl-formamide; 5.1: Swern oxidation;
DOI:10.1021/jm000410y