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

Base Information

Chemical Name:9-phenylacetyl-2-(2-fluorophenyl)-7,8,9,10-tetrahydropyrido[3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one
CAS No.:108442-31-5
Molecular Formula:C₂₂H₁₈FN₅O₂
Molecular Weight:403.416
Hs Code.:

Synonyms:9-phenylacetyl-2-(2-fluorophenyl)-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-phenylacetyl-2-(2-fluorophenyl)-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-phenylacetyl-2-(2-fluorophenyl)-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-phenylacetyl-2-(2-fluorophenyl)-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: 85.0%

: 108442-28-0
2-(2-fluorophenyl)-7,8,9,10-tetrahydropyrido[3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one

: 103-80-0
phenylacetyl chloride

: 108442-31-5
9-phenylacetyl-2-(2-fluorophenyl)-7,8,9,10-tetrahydropyrido[3,4-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)one

Guidance literature:

Reference yield:

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

: 108442-31-5
9-phenylacetyl-2-(2-fluorophenyl)-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 6 steps

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

2: 79 percent / sodium bicarbonate / butan-2-one / 2 h

3: NaOEt / ethanol / 2 h / 110 °C

4: 26 percent / tri-n-propylamine / 2-methoxy-ethanol / 16 h / Heating

5: 1.) 4 N NaOH, 2.) aq. HCl / 1.) methoxyethanol, 120 deg C, overnight

6: 79 percent / 4 h / 120 °C

With hydrogenchloride; tri-n-propylamine; sodium hydroxide; potassium tert-butylate; sodium ethanolate; sodium hydrogencarbonate; In ethanol; 2-methoxy-ethanol; butanone; tert-butyl alcohol;
DOI:10.1021/jm00113a032

Reference yield:

: 15827-80-2
4-amino-3-cyano-1,2,5,6-tetrahydropyridine

: 108442-31-5
9-phenylacetyl-2-(2-fluorophenyl)-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 5 steps

1: 79 percent / sodium bicarbonate / butan-2-one / 2 h

2: NaOEt / ethanol / 2 h / 110 °C

3: 26 percent / tri-n-propylamine / 2-methoxy-ethanol / 16 h / Heating

4: 1.) 4 N NaOH, 2.) aq. HCl / 1.) methoxyethanol, 120 deg C, overnight

5: 79 percent / 4 h / 120 °C

With hydrogenchloride; tri-n-propylamine; sodium hydroxide; sodium ethanolate; sodium hydrogencarbonate; In ethanol; 2-methoxy-ethanol; butanone;
DOI:10.1021/jm00113a032