5-(tert-butoxycarbonyl-methyl-amino)-2-methylsulfanyl-4-oxo-5,6-dihydro-4H-pyrimidine-1-carboxylic acid benzyl ester

Base Information

Chemical Name:5-(tert-butoxycarbonyl-methyl-amino)-2-methylsulfanyl-4-oxo-5,6-dihydro-4H-pyrimidine-1-carboxylic acid benzyl ester
CAS No.:554412-66-7
Molecular Formula:C₁₉H₂₅N₃O₅S
Molecular Weight:407.491
Hs Code.:

5-(<i>tert</i>-butoxycarbonyl-methyl-amino)-2-methylsulfanyl-4-oxo-5,6-dihydro-4<i>H</i>-pyrimidine-1-carboxylic acid benzyl ester

Synonyms:5-(tert-butoxycarbonyl-methyl-amino)-2-methylsulfanyl-4-oxo-5,6-dihydro-4H-pyrimidine-1-carboxylic acid benzyl ester

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Chemical Property of 5-(tert-butoxycarbonyl-methyl-amino)-2-methylsulfanyl-4-oxo-5,6-dihydro-4H-pyrimidine-1-carboxylic acid benzyl ester

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Technology Process of 5-(tert-butoxycarbonyl-methyl-amino)-2-methylsulfanyl-4-oxo-5,6-dihydro-4H-pyrimidine-1-carboxylic acid benzyl ester

There total 2 articles about 5-(tert-butoxycarbonyl-methyl-amino)-2-methylsulfanyl-4-oxo-5,6-dihydro-4H-pyrimidine-1-carboxylic acid benzyl 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:

: 501-53-1,94274-21-2
benzyl chloroformate

: 554412-62-3
methyl-(2-methylsulfanyl-4-oxo-1,4,5,6-tetrahydro-pyrimidin-5-yl)-carbamic acid tert-butyl ester

: 554412-66-7
5-(tert-butoxycarbonyl-methyl-amino)-2-methylsulfanyl-4-oxo-5,6-dihydro-4H-pyrimidine-1-carboxylic acid benzyl ester

Guidance literature:: With potassium carbonate; In acetonitrile; at 20 ℃; for 2h;
DOI:10.1016/S0040-4039(03)00226-0

Reference yield:

: 56776-34-2
N-Boc-N-methyl-dehydroalanine methyl ester

: 554412-66-7
5-(tert-butoxycarbonyl-methyl-amino)-2-methylsulfanyl-4-oxo-5,6-dihydro-4H-pyrimidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / K₂CO₃ / acetonitrile / 30 h / 20 °C

2: K₂CO₃ / acetonitrile / 2 h / 20 °C

With potassium carbonate; In acetonitrile; 1: Michael addition;
DOI:10.1016/S0040-4039(03)00226-0