N-(1-{hydroxy-[5-(1-methyl-cyclopropyl)-[1,3,4]oxadiazol-2-yl]-methyl}-2-methyl-propyl)-2-(6-oxo-2-phenyl-6H-pyrimidin-1-yl)-acetamide

Base Information

Chemical Name:N-(1-{hydroxy-[5-(1-methyl-cyclopropyl)-[1,3,4]oxadiazol-2-yl]-methyl}-2-methyl-propyl)-2-(6-oxo-2-phenyl-6H-pyrimidin-1-yl)-acetamide
CAS No.:1026395-08-3
Molecular Formula:C₂₃H₂₇N₅O₄
Molecular Weight:437.498
Hs Code.:

<i>N</i>-(1-{hydroxy-[5-(1-methyl-cyclopropyl)-[1,3,4]oxadiazol-2-yl]-methyl}-2-methyl-propyl)-2-(6-oxo-2-phenyl-6<i>H</i>-pyrimidin-1-yl)-acetamide

Synonyms:N-(1-{hydroxy-[5-(1-methyl-cyclopropyl)-[1,3,4]oxadiazol-2-yl]-methyl}-2-methyl-propyl)-2-(6-oxo-2-phenyl-6H-pyrimidin-1-yl)-acetamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(1-{hydroxy-[5-(1-methyl-cyclopropyl)-[1,3,4]oxadiazol-2-yl]-methyl}-2-methyl-propyl)-2-(6-oxo-2-phenyl-6H-pyrimidin-1-yl)-acetamide

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of N-(1-{hydroxy-[5-(1-methyl-cyclopropyl)-[1,3,4]oxadiazol-2-yl]-methyl}-2-methyl-propyl)-2-(6-oxo-2-phenyl-6H-pyrimidin-1-yl)-acetamide

There total 9 articles about N-(1-{hydroxy-[5-(1-methyl-cyclopropyl)-[1,3,4]oxadiazol-2-yl]-methyl}-2-methyl-propyl)-2-(6-oxo-2-phenyl-6H-pyrimidin-1-yl)-acetamide 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:

: 6206-25-3
methyl 1-methylcyclopropanecarboxylate

: 1026395-08-3
N-(1-{hydroxy-[5-(1-methyl-cyclopropyl)-[1,3,4]oxadiazol-2-yl]-methyl}-2-methyl-propyl)-2-(6-oxo-2-phenyl-6H-pyrimidin-1-yl)-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrazine hydrate / 28 h / Heating

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

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

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

4.1: HCl / dioxane / 2 h / 20 °C

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

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

Reference yield:

: 337969-34-3
2-(6-oxo-2-phenylhydropyrimidinyl)acetic acid

: (S)-2-Amino-3-methyl-1-[5-(1-methyl-cyclopropyl)-[1,3,4]oxadiazol-2-yl]-butan-1-ol; hydrochloride

: 1026395-08-3
N-(1-{hydroxy-[5-(1-methyl-cyclopropyl)-[1,3,4]oxadiazol-2-yl]-methyl}-2-methyl-propyl)-2-(6-oxo-2-phenyl-6H-pyrimidin-1-yl)-acetamide

Guidance literature:: With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃; for 3.5h;
DOI:10.1021/jm000410y

Reference yield:

: 72790-89-7
1-methylcyclopropane-1-carbohydrazide

: 1026395-08-3
N-(1-{hydroxy-[5-(1-methyl-cyclopropyl)-[1,3,4]oxadiazol-2-yl]-methyl}-2-methyl-propyl)-2-(6-oxo-2-phenyl-6H-pyrimidin-1-yl)-acetamide

Guidance literature:: Multi-step reaction with 4 steps

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

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

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

3.1: HCl / dioxane / 2 h / 20 °C

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

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