2-amino-6-[(cyanomethyl)sulfanyl]-4-(4-methoxyphenyl)-3,5-pyridinedicarbonitrile

Base Information

Chemical Name:2-amino-6-[(cyanomethyl)sulfanyl]-4-(4-methoxyphenyl)-3,5-pyridinedicarbonitrile
CAS No.:354784-23-9
Molecular Formula:C₁₆H₁₁N₅OS
Molecular Weight:321.362
Hs Code.:
Mol file:354784-23-9.mol

Synonyms:6-amino-2-[(cyanomethyl)thio]-4-(4-methoxyphenyl)pyridine-3,5-dicarbonitrile

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Chemical Property of 2-amino-6-[(cyanomethyl)sulfanyl]-4-(4-methoxyphenyl)-3,5-pyridinedicarbonitrile

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Technology Process of 2-amino-6-[(cyanomethyl)sulfanyl]-4-(4-methoxyphenyl)-3,5-pyridinedicarbonitrile

There total 1 articles about 2-amino-6-[(cyanomethyl)sulfanyl]-4-(4-methoxyphenyl)-3,5-pyridinedicarbonitrile 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: 69.0%

: 107-14-2
chloroacetonitrile

: 110691-01-5
6-amino-4-(4-methoxyphenyl)-2-thioxo-1,2-dihydropyridine-3,5-dicarbonitrile

: 354784-23-9
6-amino-2-[(cyanomethyl)thio]-4-(4-methoxyphenyl)pyridine-3,5-dicarbonitrile

Guidance literature:: With potassium hydroxide; In N,N-dimethyl-formamide; at 20 ℃; for 2h;
DOI:10.1002/hc.20313

Reference yield: 75.0%

: 354784-23-9
6-amino-2-[(cyanomethyl)thio]-4-(4-methoxyphenyl)pyridine-3,5-dicarbonitrile

: 476319-02-5
3,6-diamino-4-(4-methoxyphenyl)thieno[2,3-b]pyridine-2,5-dicarbonitrile

Guidance literature:: With potassium hydroxide; In ethanol; for 3h; Heating;
DOI:10.1002/hc.20313

Reference yield:

: 354784-23-9
6-amino-2-[(cyanomethyl)thio]-4-(4-methoxyphenyl)pyridine-3,5-dicarbonitrile

: 7-amino-9-(4-methoxyphenyl)-4-[(4-methylphenyl)amino]pyrido[3',2':4,5]thieno[3,2-d]pyrimidine-8-carbonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / potassium hydroxide / ethanol / 3 h / Heating

2: 60 percent / xylene / Heating

3: 63 percent / glacial acetic acid / 4 h / Heating

With potassium hydroxide; acetic acid; In ethanol; xylene;
DOI:10.1002/hc.20313