6-(4-chlorophenyl)-1,6-dihydro-2-methoxy-5-methoxycarbonyl-4-methyl-1-[(4-nitrophenyloxy)carbonyl]pyrimidine

Base Information

Chemical Name:6-(4-chlorophenyl)-1,6-dihydro-2-methoxy-5-methoxycarbonyl-4-methyl-1-[(4-nitrophenyloxy)carbonyl]pyrimidine
CAS No.:251930-59-3
Molecular Formula:C₂₁H₁₈ClN₃O₇
Molecular Weight:459.843
Hs Code.:

Synonyms:6-(4-chlorophenyl)-1,6-dihydro-2-methoxy-5-methoxycarbonyl-4-methyl-1-[(4-nitrophenyloxy)carbonyl]pyrimidine

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Chemical Property of 6-(4-chlorophenyl)-1,6-dihydro-2-methoxy-5-methoxycarbonyl-4-methyl-1-[(4-nitrophenyloxy)carbonyl]pyrimidine

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Technology Process of 6-(4-chlorophenyl)-1,6-dihydro-2-methoxy-5-methoxycarbonyl-4-methyl-1-[(4-nitrophenyloxy)carbonyl]pyrimidine

There total 4 articles about 6-(4-chlorophenyl)-1,6-dihydro-2-methoxy-5-methoxycarbonyl-4-methyl-1-[(4-nitrophenyloxy)carbonyl]pyrimidine 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: 63.0%

: 7693-46-1
4-Nitrophenyl chloroformate

: 251930-51-5
4-(4-chloro-phenyl)-2-methoxy-6-methyl-1,4-dihydro-pyrimidine-5-carboxylic acid methyl ester

: 251930-59-3
6-(4-chlorophenyl)-1,6-dihydro-2-methoxy-5-methoxycarbonyl-4-methyl-1-[(4-nitrophenyloxy)carbonyl]pyrimidine

Guidance literature:: With dmap; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1021/jm990200p

Reference yield:

: 104-88-1
4-chlorobenzaldehyde

: 251930-59-3
6-(4-chlorophenyl)-1,6-dihydro-2-methoxy-5-methoxycarbonyl-4-methyl-1-[(4-nitrophenyloxy)carbonyl]pyrimidine

Guidance literature:: Multi-step reaction with 3 steps

1: piperidine; AcOH / benzene / 8 h / Heating

2: NaHCO₃ / dimethylformamide / 16 h / 70 °C

3: 63 percent / DMAP / CH₂Cl₂ / 12 h / 20 °C

With piperidine; dmap; sodium hydrogencarbonate; acetic acid; In dichloromethane; N,N-dimethyl-formamide; benzene; 1: Condensation / 2: Condensation / 3: Carboxylation;
DOI:10.1021/jm990200p

Reference yield:

: 105-45-3
acetoacetic acid methyl ester

: 251930-59-3
6-(4-chlorophenyl)-1,6-dihydro-2-methoxy-5-methoxycarbonyl-4-methyl-1-[(4-nitrophenyloxy)carbonyl]pyrimidine

Guidance literature:: Multi-step reaction with 3 steps

1: piperidine; AcOH / benzene / 8 h / Heating

2: NaHCO₃ / dimethylformamide / 16 h / 70 °C

3: 63 percent / DMAP / CH₂Cl₂ / 12 h / 20 °C

With piperidine; dmap; sodium hydrogencarbonate; acetic acid; In dichloromethane; N,N-dimethyl-formamide; benzene; 1: Condensation / 2: Condensation / 3: Carboxylation;
DOI:10.1021/jm990200p