{1-[5-bromo-3-(2,6-difluoro-benzyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl]-3-phenyl-propyl}-carbamic acid tert-butyl ester

Base Information

• Chemical Name: {1-[5-bromo-3-(2,6-difluoro-benzyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl]-3-phenyl-propyl}-carbamic acid tert-butyl ester
• CAS No.: 732282-77-8
• Molecular Formula: C₂₇H₃₀BrF₂N₃O₄
• Molecular Weight: 578.454
• Mol file: 732282-77-8.mol

Synonyms:{1-[5-bromo-3-(2,6-difluoro-benzyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl]-3-phenyl-propyl}-carbamic acid tert-butyl ester

Chemical Property of {1-[5-bromo-3-(2,6-difluoro-benzyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl]-3-phenyl-propyl}-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of {1-[5-bromo-3-(2,6-difluoro-benzyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl]-3-phenyl-propyl}-carbamic acid tert-butyl ester

There total 1 articles about {1-[5-bromo-3-(2,6-difluoro-benzyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl]-3-phenyl-propyl}-carbamic 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:

(1S-hydroxymethyl-3-phenylpropyl)carbamic acid tert-butyl ester (116611-54-2) + 5-bromo-1-(2,6-difluoro-benzyl)-6-methyl-1H-pyrimidine-2,4-dione (352303-66-3) → {1-[5-bromo-3-(2,6-difluoro-benzyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl]-3-phenyl-propyl}-carbamic acid tert-butyl ester (732282-77-8)

Guidance literature:

With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 20 ℃; for 5h;

DOI:10.1021/jm049791w

Reference yield:

(2-fluoro-3-methoxyphenyl)boronic acid (352303-67-4) + {1-[5-bromo-3-(2,6-difluoro-benzyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl]-3-phenyl-propyl}-carbamic acid tert-butyl ester (732282-77-8) → {1-[3-(2,6-difluoro-benzyl)-5-(2-fluoro-3-methoxy-phenyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl]-3-phenyl-propyl}-carbamic acid tert-butyl ester (732282-87-0)

Guidance literature:

With barium dihydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,2-dimethoxyethane; ethanol; benzene; at 80 ℃; for 16h;

DOI:10.1021/jm049791w

Reference yield:

{1-[5-bromo-3-(2,6-difluoro-benzyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl]-3-phenyl-propyl}-carbamic acid tert-butyl ester (732282-77-8) → 3-(2-amino-4-phenyl-butyl)-1-(2,6-difluoro-benzyl)-5-(2-fluoro-3-methoxy-phenyl)-6-methyl-1H-pyrimidine-2,4-dione

Guidance literature:

Multi-step reaction with 2 steps

1: Pd(PPH₃)4; aq. Ba(OH)2 / 1,2-dimethoxy-ethane; benzene; ethanol / 16 h / 80 °C

2: TFA / CH₂Cl₂ / 1 h / 20 °C

With barium dihydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; trifluoroacetic acid; In 1,2-dimethoxyethane; ethanol; dichloromethane; benzene; 1: Suzuki coupling;

DOI:10.1021/jm049791w

upstream raw materials:

(1S-hydroxymethyl-3-phenylpropyl)carbamic acid tert-butyl ester

5-bromo-1-(2,6-difluoro-benzyl)-6-methyl-1H-pyrimidine-2,4-dione

Downstream raw materials:

{1-[3-(2,6-difluoro-benzyl)-5-(2-fluoro-3-methoxy-phenyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl]-3-phenyl-propyl}-carbamic acid tert-butyl ester