5-[4-(2-aminomethylpyrimidin-5-yl)phenyl]-4-fluoromethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester

Base Information

Chemical Name:5-[4-(2-aminomethylpyrimidin-5-yl)phenyl]-4-fluoromethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester
CAS No.:1454906-60-5
Molecular Formula:C₂₂H₂₉FN₄O₃
Molecular Weight:416.496
Hs Code.:

Synonyms:5-[4-(2-aminomethylpyrimidin-5-yl)phenyl]-4-fluoromethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester

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Chemical Property of 5-[4-(2-aminomethylpyrimidin-5-yl)phenyl]-4-fluoromethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester

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Technology Process of 5-[4-(2-aminomethylpyrimidin-5-yl)phenyl]-4-fluoromethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester

There total 4 articles about 5-[4-(2-aminomethylpyrimidin-5-yl)phenyl]-4-fluoromethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl 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:

: 1454906-59-2
5-[4-(2-cyanopyrimidin-5-yl)phenyl]-4-fluoromethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester

: 1454906-60-5
5-[4-(2-aminomethylpyrimidin-5-yl)phenyl]-4-fluoromethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 16h; under 760.051 Torr;

Reference yield:

: 1052114-46-1
tert-butyl ((1R,2S)-3-fluoro-1-hydroxy-1-(4-iodophenyl)propan-2-yl)carbamate

: 1454906-60-5
5-[4-(2-aminomethylpyrimidin-5-yl)phenyl]-4-fluoromethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: toluene-4-sulfonic acid / dichloromethane / 2 h / 20 °C / Cooling with ice

2: potassium acetate; bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane / Reflux

3: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; toluene / 16 h / 80 °C / Inert atmosphere

4: palladium 10% on activated carbon; hydrogen / methanol / 16 h / 20 °C / 760.05 Torr

With bis-triphenylphosphine-palladium(II) chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; hydrogen; potassium acetate; toluene-4-sulfonic acid; In 1,4-dioxane; methanol; dichloromethane; water; toluene;

Reference yield:

: 1454906-58-1
(4S,5R)-4-fluoromethyl-5-(4-iodophenyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester

: 1454906-60-5
5-[4-(2-aminomethylpyrimidin-5-yl)phenyl]-4-fluoromethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: potassium acetate; bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane / Reflux

2: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; toluene / 16 h / 80 °C / Inert atmosphere

3: palladium 10% on activated carbon; hydrogen / methanol / 16 h / 20 °C / 760.05 Torr

With bis-triphenylphosphine-palladium(II) chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; hydrogen; potassium acetate; In 1,4-dioxane; methanol; water; toluene;