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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250178Generated: October 27, 2026

Triphenylphosphine → 6-cyclobutyl-3-(2-fluorophenyl)-5-(2-methyl-2H-1,2,4-triazol-3-ylmethoxy)-1,2,3-triazolo[1,5-alpha]pyrimidine

https://huagongshe.com/reaction/1250178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(1-methyl-1H-1,2,4-triazol-5-yl)methanolHCID 11073377—
ReactantHCID 178518574HCID 178518574—
SolventTetrahydrofuranHCID 8028—
Product6-cyclobutyl-3-(2-fluorophenyl)-5-(2-methyl-2H-1,2,4-triazol-3-ylmethoxy)-1,2,3-triazolo[1,5-alpha]pyrimidineHCID 5442926870%

Reaction Steps

6-Cyclobutyl-3-(2-fluorophenyl)-4H-1,2,3-triazolo[1,5-α]pyrimidin-5-one (33 mg, 0.12 mmol), triphenylphosphine (76 mg, 0.29 mmol) and (2-methyl-2H-1,2,4-triazol-3-yl)methanol (37 mg, 0.29 mmol) were dissolved in dry tetrahydrofuran (1.5 ml) with stirring. Diethyl azodicarboxylate (46μl, 0.29 mmol) was added and the reaction stirred at room temperature for 16 hours before purification by preparative thin layer chromatography to afford 6-cyclobutyl-3-(2-fluorophenyl)-5-(2-methyl-2H-1,2,4-triazol-3-ylmethoxy)-1,2,3-triazolo[1,5-α]pyrimidine (31 mg, 70%) as a white crystalline solid, m.p. 181-184° C.; δH (400 MHz, d6-DMSO) 1.77-1.85 (1H, m, CH(CH2)3), 1.96-2.06 (1H, m, CH(CH2)3), 2.19-2.30 (4H, m, CH(CH2)3), 308 (1H, quintet, J=8.6 Hz, CH(CH2)3), 3.88 (3H, s, NMe, 5.65 (2H, s, OCH2), 7.34-7.38 (2H, m, ArH), 7.41-7.48 (1H, m, ArH), 7.94 (1H, s, triazole CH), 7.97 (1H, t, J=7.2 Hz, ArH), 9.25 (1H, s, pyrimidine CH); m/z (ES+) 380 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337331B1
Source datasetuspto-grants-2002_01
ORD IDord-65d87cdc3c78479b9e90412aa7673ff2
Source noteuspto-grants-2002_01