5-(4,4-difluorocyclohexyl)-2-methyl-4-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidine

Base Information

Chemical Name:5-(4,4-difluorocyclohexyl)-2-methyl-4-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidine
CAS No.:1611452-63-1
Molecular Formula:C₂₁H₂₅F₂N₃O
Molecular Weight:373.446
Hs Code.:

Synonyms:5-(4,4-difluorocyclohexyl)-2-methyl-4-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidine

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Chemical Property of 5-(4,4-difluorocyclohexyl)-2-methyl-4-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidine

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Technology Process of 5-(4,4-difluorocyclohexyl)-2-methyl-4-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidine

There total 7 articles about 5-(4,4-difluorocyclohexyl)-2-methyl-4-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidine 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: 65.0%

: 1611452-35-7
4-(2-methyl-4-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidin-5-yl)cyclohexanone

: 1611452-63-1
5-(4,4-difluorocyclohexyl)-2-methyl-4-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidine

Guidance literature:: With diethylamino-sulfur trifluoride; In dichloromethane; for 0.5h;

Reference yield:

: 1676-57-9
5-bromo-2-methylpyrimidin-4-ol

: 1611452-63-1
5-(4,4-difluorocyclohexyl)-2-methyl-4-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidine

Guidance literature:: Multi-step reaction with 5 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate / 1,4-dioxane; water / 16 h / 100 °C

2: hydrogen; palladium on activated charcoal / methanol / 20 °C

3: triphenylphosphine / tetrahydrofuran / 0.17 h / 0 - 20 °C

4: trifluoroacetic acid / 0.5 h / 20 °C

5: diethylamino-sulfur trifluoride / dichloromethane / 0.5 h

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; diethylamino-sulfur trifluoride; palladium on activated charcoal; hydrogen; potassium carbonate; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water;

Reference yield:

: 680596-79-6
4,4,5,5-tetramethyl-2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-1,3,2-dioxaborolane

: 1611452-63-1
5-(4,4-difluorocyclohexyl)-2-methyl-4-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyrimidine

Guidance literature:: Multi-step reaction with 5 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate / 1,4-dioxane; water / 16 h / 100 °C

2: hydrogen; palladium on activated charcoal / methanol / 20 °C

3: triphenylphosphine / tetrahydrofuran / 0.17 h / 0 - 20 °C

4: trifluoroacetic acid / 0.5 h / 20 °C

5: diethylamino-sulfur trifluoride / dichloromethane / 0.5 h

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; diethylamino-sulfur trifluoride; palladium on activated charcoal; hydrogen; potassium carbonate; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water;