2-(1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazol-3-yl)-6-oxo-1,6-dihydropyrimidine-5-carbonitrile

Base Information

Chemical Name:2-(1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazol-3-yl)-6-oxo-1,6-dihydropyrimidine-5-carbonitrile
CAS No.:1354041-38-5
Molecular Formula:C₁₈H₁₁FN₆O₂
Molecular Weight:362.323
Hs Code.:

Synonyms:2-(1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazol-3-yl)-6-oxo-1,6-dihydropyrimidine-5-carbonitrile

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Chemical Property of 2-(1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazol-3-yl)-6-oxo-1,6-dihydropyrimidine-5-carbonitrile

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Technology Process of 2-(1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazol-3-yl)-6-oxo-1,6-dihydropyrimidine-5-carbonitrile

There total 3 articles about 2-(1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazol-3-yl)-6-oxo-1,6-dihydropyrimidine-5-carbonitrile 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: 4.0%

: 144918-37-6,56569-41-6
1-cyano-1-ethoxycarbonyl-1-butene

: 1354044-23-7
1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazole-3-carboximidamide

: 1354041-38-5
2-(1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazol-3-yl)-4-hydroxypyrimidine-5-carbonitrile

: 1354041-60-3
ethyl 4-amino-2-(1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazol-3-yl)pyrimidine-5-carboxylate

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In ethanol; at 80 ℃; for 24h;
DOI:10.1021/acsmedchemlett.5b00479

Reference yield:

: 1354044-05-5
1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazole-3-carboximidamide hydrochloride

: 1354041-38-5
2-(1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazol-3-yl)-4-hydroxypyrimidine-5-carbonitrile

: 1354041-60-3
ethyl 4-amino-2-(1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazol-3-yl)pyrimidine-5-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: ammonium chloride; trimethylaluminum / toluene / 16 h / Inert atmosphere

2: 1,8-diazabicyclo[5.4.0]undec-7-ene / ethanol / 24 h / 80 °C

With trimethylaluminum; ammonium chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In ethanol; toluene;
DOI:10.1021/acsmedchemlett.5b00479