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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858676Generated: October 31, 2026

6-Methyl-[1,2,4]triazolo[1,5-A]pyrimidine-2-carbaldehyde → HCID 58762196, compound

https://huagongshe.com/reaction/858676

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methyl-[1,2,4]triazolo[1,5-A]pyrimidine-2-carbaldehydeHCID 58762619—
ReactantHCID 58762700HCID 58762700—
SolventMethanolHCID 887—
ProductHCID 58762196HCID 5876219620.7%

Reaction Steps

6-methyl-[1,2,4]triazolo[1,5-a]pyrimidine-2-carbaldehyde (0.88 g, 0.546 mmol) was added to a solution of example A(228) 6-cyclopentyl-6-{2-[4-hydroxy-3-(2,2,2-trifluoroethyl)phenyl]ethyl}dihydro-2H-pyran-2,4(3H)-dione (0.175 g, 0.455 mmol) and borane-dimethylamine complex (53 mg, 0.9 mmoL) in MeOH (10 mL). The reaction was stirred at room temperature for 15 hours, after which time the mixture was concentrated to a residual oil, and purified by preparatory HPLC to afford the title compound as a white solid (50 mg). 1H NMR (DMSO): δ 1.35–1.85 (brm, 8H), 2.00–2.20 (brm, 3H), 2.50 (s, 3H), 2.74 (s, 2H), 2.99(m, 2H); 3.04 (m, 2H), 3.54 (m, 3H), 6.81 (m, 2H), 7.00(s, 1H), 8.55 (s, 1H), 8.72 (s, 1H). Anal. Calcd. For C27H29O4N4F3: C, 61.14; H, 5.51; N, 9.06. Found: C, 61.21; H, 5.60; N, 9.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148226B2
Source datasetuspto-grants-2006_12
ORD IDord-7840a72ec30a4205984be44db1e8f04c
Source noteuspto-grants-2006_12