(R)-3-(2-amino-2-phenylethyl)-1-(2-fluoro-6-(trifluoromethyl)benzyl)-5-(4-(2-fluorobenzyl)piperazin-1-yl)-6-methylpyrimidine-2,4(1H,3H)-dione

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Chemical Name:(R)-3-(2-amino-2-phenylethyl)-1-(2-fluoro-6-(trifluoromethyl)benzyl)-5-(4-(2-fluorobenzyl)piperazin-1-yl)-6-methylpyrimidine-2,4(1H,3H)-dione
CAS No.:1308376-76-2
Molecular Formula:C₃₂H₃₂F₅N₅O₂
Molecular Weight:613.63
Hs Code.:

(R)-3-(2-amino-2-phenylethyl)-1-(2-fluoro-6-(trifluoromethyl)benzyl)-5-(4-(2-fluorobenzyl)piperazin-1-yl)-6-methylpyrimidine-2,4(1H,3H)-dione

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Chemical Property of (R)-3-(2-amino-2-phenylethyl)-1-(2-fluoro-6-(trifluoromethyl)benzyl)-5-(4-(2-fluorobenzyl)piperazin-1-yl)-6-methylpyrimidine-2,4(1H,3H)-dione

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Technology Process of (R)-3-(2-amino-2-phenylethyl)-1-(2-fluoro-6-(trifluoromethyl)benzyl)-5-(4-(2-fluorobenzyl)piperazin-1-yl)-6-methylpyrimidine-2,4(1H,3H)-dione

There total 5 articles about (R)-3-(2-amino-2-phenylethyl)-1-(2-fluoro-6-(trifluoromethyl)benzyl)-5-(4-(2-fluorobenzyl)piperazin-1-yl)-6-methylpyrimidine-2,4(1H,3H)-dione 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:

: C₃₇H₄₀F₅N₅O₄

: 1308376-76-2
(R)-3-(2-amino-2-phenylethyl)-1-(2-fluoro-6-(trifluoromethyl)benzyl)-5-(4-(2-fluorobenzyl)piperazin-1-yl)-6-methylpyrimidine-2,4(1H,3H)-dione

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃; for 3h;
DOI:10.1021/acs.jmedchem.6b01071

Reference yield:

: 830346-49-1
{(R)-2-[5-bromo-3-(2-fluoro-6-trifluoromethyl-benzyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl]-1-phenyl-ethyl}-carbamic acid tert-butyl ester

: 1308376-76-2
(R)-3-(2-amino-2-phenylethyl)-1-(2-fluoro-6-(trifluoromethyl)benzyl)-5-(4-(2-fluorobenzyl)piperazin-1-yl)-6-methylpyrimidine-2,4(1H,3H)-dione

Guidance literature:: Multi-step reaction with 4 steps

1: acetonitrile / 2 h / 120 °C / Microwave irradiation

2: palladium 10% on activated carbon; hydrogen / methanol / 5 h / 20 °C / 760.05 Torr

3: potassium carbonate / acetonitrile / 3 h / 20 - 60 °C

4: trifluoroacetic acid / dichloromethane / 3 h / 0 - 20 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; trifluoroacetic acid; In methanol; dichloromethane; acetonitrile;
DOI:10.1021/acs.jmedchem.6b01071

Reference yield:

: 1308375-89-4
{(R)-2-[5-(4-benzyl-piperazin-1-yl)-3-(2-fluoro-6-trifluoromethyl-benzyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl]-1-phenyl-ethyl}-carbamic acid tert-butyl ester

: 1308376-76-2
(R)-3-(2-amino-2-phenylethyl)-1-(2-fluoro-6-(trifluoromethyl)benzyl)-5-(4-(2-fluorobenzyl)piperazin-1-yl)-6-methylpyrimidine-2,4(1H,3H)-dione

Guidance literature:: Multi-step reaction with 3 steps

1: palladium 10% on activated carbon; hydrogen / methanol / 5 h / 20 °C / 760.05 Torr

2: potassium carbonate / acetonitrile / 3 h / 20 - 60 °C

3: trifluoroacetic acid / dichloromethane / 3 h / 0 - 20 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; trifluoroacetic acid; In methanol; dichloromethane; acetonitrile;
DOI:10.1021/acs.jmedchem.6b01071