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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858759Generated: October 26, 2026

(5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)methanol → 5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine-2-carbaldehyde

https://huagongshe.com/reaction/858759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)methanolHCID 44141733—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine-2-carbaldehydeHCID 2363522677%

Reaction Steps

A slurry of 5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-methanol (0.3 g, 1.7 mmol) from Step 2 above and IBX (1.4 g, 5.0 mmol) in 1,2-dichloroethane (22 mL) was stirred at 80° C. for 18 hours. The reaction was cooled to room temperature, and diluted with 100 mL CH2Cl2. After the solids were removed by filtration, the solvent was removed by rotary evaporation to give a yellow solid. The solid was purified by flash chromatography to give the desired product (229 mg, 77% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148226B2
Source datasetuspto-grants-2006_12
ORD IDord-23fecfa1330348d8bc92473e4c6c3aa1
Source noteuspto-grants-2006_12