(R)-3-((1r,4R)-4-(6-amino-5-bromopyridin-3-yl)cyclohexyl)-5,5-dimethyl-4-phenyloxazolidin-2-one

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Chemical Name:(R)-3-((1r,4R)-4-(6-amino-5-bromopyridin-3-yl)cyclohexyl)-5,5-dimethyl-4-phenyloxazolidin-2-one
CAS No.:1456506-72-1
Molecular Formula:C₂₂H₂₆BrN₃O₂
Molecular Weight:444.371
Hs Code.:

Synonyms:(R)-3-((1r,4R)-4-(6-amino-5-bromopyridin-3-yl)cyclohexyl)-5,5-dimethyl-4-phenyloxazolidin-2-one

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Chemical Property of (R)-3-((1r,4R)-4-(6-amino-5-bromopyridin-3-yl)cyclohexyl)-5,5-dimethyl-4-phenyloxazolidin-2-one

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Technology Process of (R)-3-((1r,4R)-4-(6-amino-5-bromopyridin-3-yl)cyclohexyl)-5,5-dimethyl-4-phenyloxazolidin-2-one

There total 4 articles about (R)-3-((1r,4R)-4-(6-amino-5-bromopyridin-3-yl)cyclohexyl)-5,5-dimethyl-4-phenyloxazolidin-2-one 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:

: 1456506-75-4
(R)-3-((1r,4R)-4-(6-aminopyridin-3-yl)cyclohexyl)-5,5-dimethyl-4-phenyloxazolidin-2-one

: 1456506-72-1
(R)-3-((1r,4R)-4-(6-amino-5-bromopyridin-3-yl)cyclohexyl)-5,5-dimethyl-4-phenyloxazolidin-2-one

Guidance literature:: With N-Bromosuccinimide; In dichloromethane; at 0 ℃; for 1h;

Reference yield:

: 827614-64-2
2-aminopyridine-5-boronic acid pinacol ester

: 1456506-72-1
(R)-3-((1r,4R)-4-(6-amino-5-bromopyridin-3-yl)cyclohexyl)-5,5-dimethyl-4-phenyloxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane / 1 h / 100 °C / Inert atmosphere; Sealed tube; Microwave irradiation

2.1: palladium 10% on activated carbon; hydrogen / methanol / 50 °C / 2327.23 Torr

2.2: Chiralpak AD / Resolution of racemate

3.1: N-Bromosuccinimide / dichloromethane / 1 h / 0 °C

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; hydrogen; sodium carbonate; In 1,4-dioxane; methanol; dichloromethane;

Reference yield:

: 1456506-73-2
3-(4-(6-aminopyridin-3-yl)cyclohex-3-en-1-yl)-5,5-dimethyl-4-phenyloxazolidin-2-one

: 1456506-72-1
(R)-3-((1r,4R)-4-(6-amino-5-bromopyridin-3-yl)cyclohexyl)-5,5-dimethyl-4-phenyloxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: palladium 10% on activated carbon; hydrogen / methanol / 50 °C / 2327.23 Torr

1.2: Chiralpak AD / Resolution of racemate

2.1: N-Bromosuccinimide / dichloromethane / 1 h / 0 °C

With N-Bromosuccinimide; palladium 10% on activated carbon; hydrogen; In methanol; dichloromethane;