9-benzyl-2-(4-chlorophenyl)-7,8,9,10-tetrahydropyrido [3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one

Base Information

Chemical Name:9-benzyl-2-(4-chlorophenyl)-7,8,9,10-tetrahydropyrido [3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one
CAS No.:108461-24-1
Molecular Formula:C₂₁H₁₈ClN₅O
Molecular Weight:391.86
Hs Code.:

Synonyms:9-benzyl-2-(4-chlorophenyl)-7,8,9,10-tetrahydropyrido [3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one

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Chemical Property of 9-benzyl-2-(4-chlorophenyl)-7,8,9,10-tetrahydropyrido [3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one

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Technology Process of 9-benzyl-2-(4-chlorophenyl)-7,8,9,10-tetrahydropyrido [3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one

There total 6 articles about 9-benzyl-2-(4-chlorophenyl)-7,8,9,10-tetrahydropyrido [3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one 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: 54.0%

: 108461-24-1
9-benzyl-2-(4-chlorophenyl)-7,8,9,10-tetrahydropyrido [3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one

Guidance literature:

Reference yield: 17.0%

: 108442-53-1
(1-Benzyl-5-cyano-1,2,3,6-tetrahydro-pyridin-4-yl)-carbamic acid ethyl ester

: 536-40-3
4-chlorobenzoic acid hydrazide

: 108461-24-1
9-benzyl-2-(4-chlorophenyl)-7,8,9,10-tetrahydropyrido [3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl acetamide; at 150 ℃; for 16h;
DOI:10.1021/jm00113a032

Reference yield:

: 111-94-4
3,3'-Iminodipropionitrile

: 108461-24-1
9-benzyl-2-(4-chlorophenyl)-7,8,9,10-tetrahydropyrido [3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one

Guidance literature:: Multi-step reaction with 4 steps

1: NaHCO₃ / ethanol / Ambient temperature

2: KOt-Bu / 2-methyl-propan-2-ol

3: 31 percent / NaOEt / ethanol / a) reflux, 4 h, b) RT, 16 h

4: 17 percent / ethyldiisopropylamine / N,N-dimethyl-acetamide / 16 h / 150 °C

With potassium tert-butylate; sodium ethanolate; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; In ethanol; N,N-dimethyl acetamide; tert-butyl alcohol;
DOI:10.1021/jm00113a032