4-(5-chlorothiophen-2-yl)-6-ethyl-N-(4-fluorophenyl)-1,3,5-triazin-2-amine

Base Information

Chemical Name:4-(5-chlorothiophen-2-yl)-6-ethyl-N-(4-fluorophenyl)-1,3,5-triazin-2-amine
CAS No.:1606973-22-1
Molecular Formula:C₁₅H₁₂ClFN₄S
Molecular Weight:334.804
Hs Code.:

Synonyms:4-(5-chlorothiophen-2-yl)-6-ethyl-N-(4-fluorophenyl)-1,3,5-triazin-2-amine

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Chemical Property of 4-(5-chlorothiophen-2-yl)-6-ethyl-N-(4-fluorophenyl)-1,3,5-triazin-2-amine

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Technology Process of 4-(5-chlorothiophen-2-yl)-6-ethyl-N-(4-fluorophenyl)-1,3,5-triazin-2-amine

There total 3 articles about 4-(5-chlorothiophen-2-yl)-6-ethyl-N-(4-fluorophenyl)-1,3,5-triazin-2-amine 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:

: 50478-16-5
5-chlorothiophene-2-carbonitrile

: 1606973-22-1
4-(5-chlorothiophen-2-yl)-6-ethyl-N-(4-fluorophenyl)-1,3,5-triazin-2-amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium methylate / methanol / 4 h / 20 °C

1.2: Inert atmosphere

2.1: trichlorophosphate / acetonitrile / 70 °C / Inert atmosphere

3.1: acetic acid / 1 h / 100 °C

With sodium methylate; acetic acid; trichlorophosphate; In methanol; acetonitrile;
DOI:10.1016/j.bmcl.2014.06.002

Reference yield:

: 1637216-96-6
C₉H₇Cl₂N₃S

: 371-40-4
4-fluoroaniline

: 1606973-22-1
4-(5-chlorothiophen-2-yl)-6-ethyl-N-(4-fluorophenyl)-1,3,5-triazin-2-amine

Guidance literature:: With acetic acid; at 100 ℃; for 1h;
DOI:10.1016/j.bmcl.2014.06.002

Reference yield:

: 1606978-12-4
5-chloro-N-cyanothiophene-2-carboximidamide

: 1606973-22-1
4-(5-chlorothiophen-2-yl)-6-ethyl-N-(4-fluorophenyl)-1,3,5-triazin-2-amine

Guidance literature:: Multi-step reaction with 2 steps

1: trichlorophosphate / acetonitrile / 70 °C / Inert atmosphere

2: acetic acid / 1 h / 100 °C

With acetic acid; trichlorophosphate; In acetonitrile;
DOI:10.1016/j.bmcl.2014.06.002