N-[4-(aminosulfonyl)phenyl]-5-cyano-6-({2-[(4-ethylphenyl)amino]-2-oxoethyl}thio)-4-(2-furyl)-2-methyl-1,4-dihydropyridine-3-carboxamide

Base Information

Chemical Name:N-[4-(aminosulfonyl)phenyl]-5-cyano-6-({2-[(4-ethylphenyl)amino]-2-oxoethyl}thio)-4-(2-furyl)-2-methyl-1,4-dihydropyridine-3-carboxamide
CAS No.:701245-18-3
Molecular Formula:C₂₈H₂₇N₅O₅S₂
Molecular Weight:577.685
Hs Code.:

Synonyms:N-[4-(aminosulfonyl)phenyl]-5-cyano-6-({2-[(4-ethylphenyl)amino]-2-oxoethyl}thio)-4-(2-furyl)-2-methyl-1,4-dihydropyridine-3-carboxamide

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Chemical Property of N-[4-(aminosulfonyl)phenyl]-5-cyano-6-({2-[(4-ethylphenyl)amino]-2-oxoethyl}thio)-4-(2-furyl)-2-methyl-1,4-dihydropyridine-3-carboxamide

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Technology Process of N-[4-(aminosulfonyl)phenyl]-5-cyano-6-({2-[(4-ethylphenyl)amino]-2-oxoethyl}thio)-4-(2-furyl)-2-methyl-1,4-dihydropyridine-3-carboxamide

There total 3 articles about N-[4-(aminosulfonyl)phenyl]-5-cyano-6-({2-[(4-ethylphenyl)amino]-2-oxoethyl}thio)-4-(2-furyl)-2-methyl-1,4-dihydropyridine-3-carboxamide 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: 84.0%

: 1448815-86-8
N-methylmorpholinium 5-({[4-(aminosulfonyl)phenyl]amino}carbonyl)-3-cyano-4-(2-furyl)-6-methyl-1,4-dihydropyridine-2-thiolate

: 20172-36-5
α-chloro-N-(p-ethylphenyl)acetamide

: 701245-18-3
N-[4-(aminosulfonyl)phenyl]-5-cyano-6-({2-[(4-ethylphenyl)amino]-2-oxoethyl}thio)-4-(2-furyl)-2-methyl-1,4-dihydropyridine-3-carboxamide

Guidance literature:: With potassium hydroxide; In ethanol; water; at 25 - 30 ℃; for 1h; regioselective reaction; Inert atmosphere;
DOI:10.1021/ml400226s

Reference yield:

: 39145-34-1
2-furfurylidenecyanothioacetamide

: 701245-18-3
N-[4-(aminosulfonyl)phenyl]-5-cyano-6-({2-[(4-ethylphenyl)amino]-2-oxoethyl}thio)-4-(2-furyl)-2-methyl-1,4-dihydropyridine-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol / 20 °C / Inert atmosphere

2: potassium hydroxide / ethanol; water / 1 h / 25 - 30 °C / Inert atmosphere

With potassium hydroxide; In ethanol; water;
DOI:10.1021/ml400226s

Reference yield:

: 63-74-1
sulfanilamide

: 701245-18-3
N-[4-(aminosulfonyl)phenyl]-5-cyano-6-({2-[(4-ethylphenyl)amino]-2-oxoethyl}thio)-4-(2-furyl)-2-methyl-1,4-dihydropyridine-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: 4-methyl-morpholine / acetone / 1 h / Reflux; Inert atmosphere

2: ethanol / 20 °C / Inert atmosphere

3: potassium hydroxide / ethanol; water / 1 h / 25 - 30 °C / Inert atmosphere

With 4-methyl-morpholine; potassium hydroxide; In ethanol; water; acetone;
DOI:10.1021/ml400226s