5-(chloromethyl)-4-[N-(4-ethoxyphenyl)amino]-6-methyl-2-phenylpyrimidine

Base Information

Chemical Name:5-(chloromethyl)-4-[N-(4-ethoxyphenyl)amino]-6-methyl-2-phenylpyrimidine
CAS No.:164927-17-7
Molecular Formula:C₂₀H₂₀ClN₃O
Molecular Weight:353.851
Hs Code.:

Synonyms:5-(chloromethyl)-4-[N-(4-ethoxyphenyl)amino]-6-methyl-2-phenylpyrimidine

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Chemical Property of 5-(chloromethyl)-4-[N-(4-ethoxyphenyl)amino]-6-methyl-2-phenylpyrimidine

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Technology Process of 5-(chloromethyl)-4-[N-(4-ethoxyphenyl)amino]-6-methyl-2-phenylpyrimidine

There total 5 articles about 5-(chloromethyl)-4-[N-(4-ethoxyphenyl)amino]-6-methyl-2-phenylpyrimidine 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: 95.3%

: 5-hydroxymethyl-6-methyl-2-phenyl-4-(4'-ethoxyphenylamino)-pyrimidine

: 164927-17-7
5-(chloromethyl)-4-[N-(4-ethoxyphenyl)amino]-6-methyl-2-phenylpyrimidine

Guidance literature:: With sulfuryl dichloride; In benzene; for 2h;

Reference yield:

: 156-43-4
4-Ethoxyaniline

: 164927-17-7
5-(chloromethyl)-4-[N-(4-ethoxyphenyl)amino]-6-methyl-2-phenylpyrimidine

Guidance literature:: Multi-step reaction with 3 steps

1: neat (no solvent) / 4 h / Heating

2: lithium aluminium tetrahydride / tetrahydrofuran

3: thionyl chloride / benzene / 24 h / 20 °C

With lithium aluminium tetrahydride; thionyl chloride; In tetrahydrofuran; benzene;

Reference yield:

: 94037-16-8
ethyl 6-[(4-ethoxyphenyl)amino]-4-methyl-2-phenylpyrimidine-5-carboxylate

: 164927-17-7
5-(chloromethyl)-4-[N-(4-ethoxyphenyl)amino]-6-methyl-2-phenylpyrimidine

Guidance literature:: Multi-step reaction with 2 steps

1: lithium aluminium tetrahydride / tetrahydrofuran

2: thionyl chloride / benzene / 24 h / 20 °C

With lithium aluminium tetrahydride; thionyl chloride; In tetrahydrofuran; benzene;