3-(4-methoxyphenyl)-2-(N-methylbenzylamino)-5-phenyl-1,3-thiazolium-4-olate

Base Information

Chemical Name:3-(4-methoxyphenyl)-2-(N-methylbenzylamino)-5-phenyl-1,3-thiazolium-4-olate
CAS No.:173094-32-1
Molecular Formula:C₂₄H₂₂N₂O₂S
Molecular Weight:402.517
Hs Code.:

Synonyms:3-(4-methoxyphenyl)-2-(N-methylbenzylamino)-5-phenyl-1,3-thiazolium-4-olate

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Chemical Property of 3-(4-methoxyphenyl)-2-(N-methylbenzylamino)-5-phenyl-1,3-thiazolium-4-olate

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Technology Process of 3-(4-methoxyphenyl)-2-(N-methylbenzylamino)-5-phenyl-1,3-thiazolium-4-olate

There total 5 articles about 3-(4-methoxyphenyl)-2-(N-methylbenzylamino)-5-phenyl-1,3-thiazolium-4-olate 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:

: 4870-65-9,31302-84-8
2-bromophenylacetic acid

: 173094-32-1
3-(4-methoxyphenyl)-2-(N-methylbenzylamino)-5-phenyl-1,3-thiazolium-4-olate

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / benzene / 15 h / Ambient temperature

2: Ac₂O, Et₃N

With acetic anhydride; triethylamine; In benzene;
DOI:10.1021/jo952275g

Reference yield:

: 103-67-3
benzyl-methyl-amine

: 173094-32-1
3-(4-methoxyphenyl)-2-(N-methylbenzylamino)-5-phenyl-1,3-thiazolium-4-olate

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / diethyl ether / 0 °C

2: Et₃N / benzene / 15 h / Ambient temperature

3: Ac₂O, Et₃N

With acetic anhydride; triethylamine; In diethyl ether; benzene;
DOI:10.1021/jo952275g

Reference yield:

: 2284-20-0
4-Methoxyphenyl isothiocyanate

: 173094-32-1
3-(4-methoxyphenyl)-2-(N-methylbenzylamino)-5-phenyl-1,3-thiazolium-4-olate

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / diethyl ether / 0 °C

2: Et₃N / benzene / 15 h / Ambient temperature

3: Ac₂O, Et₃N

With acetic anhydride; triethylamine; In diethyl ether; benzene;
DOI:10.1021/jo952275g