1-tert-butyl 5-ethyl 4-p-methoxyphenyl-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate

Base Information

Chemical Name:1-tert-butyl 5-ethyl 4-p-methoxyphenyl-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate
CAS No.:1337541-33-9
Molecular Formula:C₂₆H₃₀N₂O₅
Molecular Weight:450.535
Hs Code.:

Synonyms:1-tert-butyl 5-ethyl 4-p-methoxyphenyl-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate

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Chemical Property of 1-tert-butyl 5-ethyl 4-p-methoxyphenyl-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate

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Technology Process of 1-tert-butyl 5-ethyl 4-p-methoxyphenyl-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate

There total 6 articles about 1-tert-butyl 5-ethyl 4-p-methoxyphenyl-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate 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: 92.0%

: 1337541-30-6
1-tert-butyl 5-ethyl 4-chloro-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate

: 5720-07-0
4-methoxyphenylboronic acid

: 1337541-33-9
1-tert-butyl 5-ethyl 4-p-methoxyphenyl-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; caesium carbonate; In N,N-dimethyl acetamide; at 60 ℃; for 3h; Inert atmosphere;
DOI:10.3987/COM-11-12244

Reference yield:

: 100416-57-7
ethyl 6-chloro-2-methyl-4-phenyl-1,4-dihydropyrimidine-5-carboxylate

: 1337541-33-9
1-tert-butyl 5-ethyl 4-p-methoxyphenyl-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0 - 20 °C / Inert atmosphere

2: bis-triphenylphosphine-palladium(II) chloride; caesium carbonate / N,N-dimethyl acetamide / 3 h / 60 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; sodium hydride; caesium carbonate; In N,N-dimethyl acetamide; N,N-dimethyl-formamide; mineral oil; 2: Suzuki-Miyaura cross-coupling;
DOI:10.3987/COM-11-12244

Reference yield:

: 96962-33-3
ethyl 2-methyl-4-phenyl-1,4,5,6-tetrahydropyrimidin-6-one-5-carboxylate

: 1337541-33-9
1-tert-butyl 5-ethyl 4-p-methoxyphenyl-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: P,P-dichlorophenylphosphine oxide / 5 h / 110 °C / Inert atmosphere

2: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0 - 20 °C / Inert atmosphere

3: bis-triphenylphosphine-palladium(II) chloride; caesium carbonate / N,N-dimethyl acetamide / 3 h / 60 °C / Inert atmosphere

With P,P-dichlorophenylphosphine oxide; bis-triphenylphosphine-palladium(II) chloride; sodium hydride; caesium carbonate; In N,N-dimethyl acetamide; N,N-dimethyl-formamide; mineral oil; 3: Suzuki-Miyaura cross-coupling;
DOI:10.3987/COM-11-12244