6-cyclobutyl-3-(2-fluorophenyl)-4H-1,2,3-triazolo[1,5-a]pyrimidin-5-one

Base Information

Chemical Name:6-cyclobutyl-3-(2-fluorophenyl)-4H-1,2,3-triazolo[1,5-a]pyrimidin-5-one
CAS No.:252369-31-6
Molecular Formula:C₁₅H₁₃FN₄O
Molecular Weight:284.293
Hs Code.:

Synonyms:6-cyclobutyl-3-(2-fluorophenyl)-4H-1,2,3-triazolo[1,5-a]pyrimidin-5-one

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Chemical Property of 6-cyclobutyl-3-(2-fluorophenyl)-4H-1,2,3-triazolo[1,5-a]pyrimidin-5-one

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Technology Process of 6-cyclobutyl-3-(2-fluorophenyl)-4H-1,2,3-triazolo[1,5-a]pyrimidin-5-one

There total 4 articles about 6-cyclobutyl-3-(2-fluorophenyl)-4H-1,2,3-triazolo[1,5-a]pyrimidin-5-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: 62.0%

: 252369-30-5
N-[3-benzenesulfinylmethyl-5-(2-fluorophenyl)-3H-1,2,3-triazol-4-yl]-2-chloro-2-cyclobutylacetamide

: 252369-31-6
6-cyclobutyl-3-(2-fluorophenyl)-4H-1,2,3-triazolo[1,5-a]pyrimidin-5-one

Guidance literature:: With potassium hexamethylsilazane; In tetrahydrofuran; toluene; at -78 - -20 ℃;
DOI:10.1055/s-2001-13354

Reference yield:

: 252369-29-2
2-chloro-2-cyclobutyl-N-[5-(2-fluorophenyl)-3-phenylsulfenylmethyl-3H-1,2,3-triazol-4-yl]acetamide

: 252369-31-6
6-cyclobutyl-3-(2-fluorophenyl)-4H-1,2,3-triazolo[1,5-a]pyrimidin-5-one

Guidance literature:: Multi-step reaction with 2 steps

1: O₃ / CH₂Cl₂ / -78 °C

2: 62 percent / KHMDS / toluene; tetrahydrofuran / -78 - -20 °C

With potassium hexamethylsilazane; ozone; In tetrahydrofuran; dichloromethane; toluene; 2: Dimroth rearrangement;
DOI:10.1055/s-2001-13354

Reference yield:

: 326-62-5
2-fluorophenyl acetonitrile

: 252369-31-6
6-cyclobutyl-3-(2-fluorophenyl)-4H-1,2,3-triazolo[1,5-a]pyrimidin-5-one

Guidance literature:: Multi-step reaction with 4 steps

1: 29 percent / K₂CO₃ / dimethylsulfoxide / 16 h / 20 °C

2: 31 percent / pyridine / dimethylformamide / 0 °C

3: O₃ / CH₂Cl₂ / -78 °C

4: 62 percent / KHMDS / toluene; tetrahydrofuran / -78 - -20 °C

With pyridine; potassium hexamethylsilazane; potassium carbonate; ozone; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene; 4: Dimroth rearrangement;
DOI:10.1055/s-2001-13354