2-[(E)-2-(6-fluoro-3-methylquinoxalin-2-yl)vinyl]-N-(trans-4-methoxycyclohexyl)-6-pyrrolidin-1-ylpyrimidin-4-amine

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Chemical Name:2-[(E)-2-(6-fluoro-3-methylquinoxalin-2-yl)vinyl]-N-(trans-4-methoxycyclohexyl)-6-pyrrolidin-1-ylpyrimidin-4-amine
CAS No.:1214253-93-6
Molecular Formula:C₂₆H₃₁FN₆O
Molecular Weight:462.57
Hs Code.:

Synonyms:2-[(E)-2-(6-fluoro-3-methylquinoxalin-2-yl)vinyl]-N-(trans-4-methoxycyclohexyl)-6-pyrrolidin-1-ylpyrimidin-4-amine

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Chemical Property of 2-[(E)-2-(6-fluoro-3-methylquinoxalin-2-yl)vinyl]-N-(trans-4-methoxycyclohexyl)-6-pyrrolidin-1-ylpyrimidin-4-amine

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Technology Process of 2-[(E)-2-(6-fluoro-3-methylquinoxalin-2-yl)vinyl]-N-(trans-4-methoxycyclohexyl)-6-pyrrolidin-1-ylpyrimidin-4-amine

There total 5 articles about 2-[(E)-2-(6-fluoro-3-methylquinoxalin-2-yl)vinyl]-N-(trans-4-methoxycyclohexyl)-6-pyrrolidin-1-ylpyrimidin-4-amine 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:

: 111300-06-2
trans-tert-butyl 4-hydroxycyclohexylcarbamate

: 1214253-93-6
2-[(E)-2-(6-fluoro-3-methylquinoxalin-2-yl)vinyl]-N-(trans-4-methoxycyclohexyl)-6-pyrrolidin-1-ylpyrimidin-4-amine

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydride; 15-crown-5 / tetrahydrofuran; mineral oil / 2 h / 0 °C

2: hydrogenchloride / 1,4-dioxane / 20 h / 0 °C

3: potassium hydroxide; XPhos / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / tert-butyl alcohol / 12 h / 80 °C

With hydrogenchloride; 15-crown-5; sodium hydride; potassium hydroxide; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; mineral oil; tert-butyl alcohol;

Reference yield:

: 19875-05-9
4,6-dichloro-2-(chloromethyl) pyrimidine

: 1214253-93-6
2-[(E)-2-(6-fluoro-3-methylquinoxalin-2-yl)vinyl]-N-(trans-4-methoxycyclohexyl)-6-pyrrolidin-1-ylpyrimidin-4-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / N,N-dimethyl-formamide / -2 - 0 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.67 h / 0 °C

2.2: 1 h / 20 °C

3.1: potassium tert-butylate / N,N-dimethyl-formamide; tetrahydrofuran / 0.5 h / 0 °C

3.2: 1 h / -78 °C

4.1: potassium hydroxide; XPhos / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / tert-butyl alcohol / 12 h / 80 °C

With potassium tert-butylate; sodium hydride; triethylamine; potassium hydroxide; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil; tert-butyl alcohol;

Reference yield:

: 760958-17-6
tert-butyl ((1r,4r)-4-methoxycyclohexyl)carbamate

: 1214253-93-6
2-[(E)-2-(6-fluoro-3-methylquinoxalin-2-yl)vinyl]-N-(trans-4-methoxycyclohexyl)-6-pyrrolidin-1-ylpyrimidin-4-amine

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / 1,4-dioxane / 20 h / 0 °C

2: potassium hydroxide; XPhos / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / tert-butyl alcohol / 12 h / 80 °C

With hydrogenchloride; potassium hydroxide; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In 1,4-dioxane; tert-butyl alcohol;