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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181287Generated: November 2, 2026

Triethylamine → 2-Furan-2-yl-5-[4-(5-methyl-isoxazol-3-ylmethyl)-piperazin-1-yl]-[1,2,4]triazolo[1,5-a][1,3,5]triazin-7-ylamine

https://huagongshe.com/reaction/1181287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonateHCID 85257—
Reactant2-Furan-2-yl-5-piperazin-1-yl-[1,2,4]triazolo[1,5-a][1,3,5]triazin-7-ylamineHCID 11449031—
ReactantMethanesulfonic acid 5-methyl-isoxazol-3-ylmethyl esterHCID 57476926—
SolventAcetonitrileHCID 6342—
Product2-Furan-2-yl-5-[4-(5-methyl-isoxazol-3-ylmethyl)-piperazin-1-yl]-[1,2,4]triazolo[1,5-a][1,3,5]triazin-7-ylamineHCID 11188193—

Reaction Steps

The mesylate derivative from subpart (a) above (0.28 mmol) was added to a solution of 2-furan-2-yl-5-piperazin-1-yl-[1,2,4]triazolo[1,5-a][1,3,5]triazin-7-ylamine (0.14 mmol; see Example 1(a) above) and Et3N (0.3 mmol) in 3 mL of CH3CN. The resulting reaction mixture was stirred at room temperature for 18 hours. It was then concentrated and purified by preparative HPLC using a mixture of aqueous CH3CN that has been buffered with 0.1% TFA.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285550B2
Source datasetuspto-grants-2007_10
ORD IDord-c71fd56e090c492ab1642de83a7b04ab
Source noteuspto-grants-2007_10