5-Benzylsulfanyl-2,6-dimethoxy-pyrimidine-4-carboxylic acid (4-methoxy-phenyl)-amide

Base Information

Chemical Name:5-Benzylsulfanyl-2,6-dimethoxy-pyrimidine-4-carboxylic acid (4-methoxy-phenyl)-amide
CAS No.:158094-19-0
Molecular Formula:C₂₁H₂₁N₃O₄S
Molecular Weight:411.481
Hs Code.:

Synonyms:5-Benzylsulfanyl-2,6-dimethoxy-pyrimidine-4-carboxylic acid (4-methoxy-phenyl)-amide

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Chemical Property of 5-Benzylsulfanyl-2,6-dimethoxy-pyrimidine-4-carboxylic acid (4-methoxy-phenyl)-amide

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Technology Process of 5-Benzylsulfanyl-2,6-dimethoxy-pyrimidine-4-carboxylic acid (4-methoxy-phenyl)-amide

There total 1 articles about 5-Benzylsulfanyl-2,6-dimethoxy-pyrimidine-4-carboxylic acid (4-methoxy-phenyl)-amide 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:

: 3012-37-1
benzyl thiocyanate

: 155185-59-4
5-Bromo-2,6-dimethoxy-pyrimidine-4-carboxylic acid (4-methoxy-phenyl)-amide

: 158094-19-0
5-Benzylsulfanyl-2,6-dimethoxy-pyrimidine-4-carboxylic acid (4-methoxy-phenyl)-amide

Guidance literature:: With n-butyllithium; sodium hydride; Yield given. Multistep reaction;
DOI:10.1016/S0040-4039(00)61393-X

Reference yield: 66.0%

: 158094-19-0
5-Benzylsulfanyl-2,6-dimethoxy-pyrimidine-4-carboxylic acid (4-methoxy-phenyl)-amide

: 155185-62-9
2,6-Dimethoxy-5-phenylmethanesulfinyl-pyrimidine-4-carboxylic acid (4-methoxy-phenyl)-amide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 ℃;
DOI:10.1021/jm00045a012

Reference yield:

: 158094-19-0
5-Benzylsulfanyl-2,6-dimethoxy-pyrimidine-4-carboxylic acid (4-methoxy-phenyl)-amide

: 5,7-Dimethoxy-2-(4-methoxy-phenyl)-isothiazolo[4,5-d]pyrimidin-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 66 percent / m-CPBA / CH₂Cl₂ / 0 °C

2: 67 percent / trichloroacetyl chloride / CH₂Cl₂ / 1.17 h / 25 °C

With 3-chloro-benzenecarboperoxoic acid; trifluoroacetyl chloride; In dichloromethane;
DOI:10.1021/jm00045a012