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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453150Generated: October 30, 2026

6-Ethyl[1,2,4]triazolo[1,5-a]pyrimidine-2-carboxaldehyde → HCID 57477231, compound

https://huagongshe.com/reaction/1453150

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Ethyl[1,2,4]triazolo[1,5-a]pyrimidine-2-carboxaldehydeHCID 60125018—
ReactantHCID 68866297HCID 68866297—
SolventMethanolHCID 887—
ProductHCID 57477231HCID 57477231—

Reaction Steps

A solution of 2-{4-[2-(2-Cyclopentyl-4-hydroxy-6-oxo-3,6-dihydro-2H-pyran-2-yl)-ethyl]-2,6-difluoro-phenyl}-2-methyl-propionitrile (272 mg, 0.7 mmol) in anhydrous MeOH (1.5 mL) was treated with 6-ethyl-[1,2,4]triazolo[1,5-a]pyrimidine-2-carbaldehyde (324 mg, 2.0 mmol), followed by borane-dimethylamine complex (191.7 mg, 1.05 mmol) at room temperature. The reaction was stirred for 12 hours. The precipitate was removed by filtration, and the filtrate was concentrated to a crude oil. The crude oil was purified by flash chromatography (25 g SiO2, 1:3:1:0 (93.5% ethyl acetate, 6% methanol, 0.5% acetic acid):(81.5% hexanes, 12% ethyl acetate, 6% methanol, 0.5% acetic acid)) to give product as an oil. It was further purified by preparatory HPLC. Yield: 19.0 mg, 8.0%. 1H NMR (CDCl3) δ: 1.37 (t, J=3.75 Hz, 3H)), 1.48-1.75 (m, 8H), 1.84 (s, 6H), 1.91-2.02 (m, 2H), 2.32-2.49 (m, 3H), 2.61-2.70 (m, 2H), 2.79-2.86 (m, 2H), 4.10 (s, 2H), 6.69 (d, J=10.86 Hz, 2H), 8.62 (s, 1H), 8.73 (s, 1H). MS (ESI): 548 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473790B2
Source datasetuspto-grants-2009_01
ORD IDord-a95f9627156c4c6db9e154e04f5dafb0
Source noteuspto-grants-2009_01