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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60146Generated: October 26, 2026

Diisopropylethylamine → Methyl 2-amino-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylate

https://huagongshe.com/reaction/60146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl isothiocyanatoformateHCID 85320—
ReactantMethyl 2-aminopyridine-4-carboxylateHCID 236984—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 2-amino-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylateHCID 68474008—

Reaction Steps

Ethoxycarbonyl isothiocyanate (9.0 g) was added to a 1,4-dioxane (100 ml) suspension of 2-aminopyridine-4-carboxylic acid methyl ester (10 g) at an internal temperature of 19° C. to 23° C. over 20 minutes. The obtained mixture was stirred for 90 minutes at the same temperature as described above, and was then concentrated under reduced pressure to obtain a crude product. The obtained crude product was added to a mixed suspension of methanol (70 ml) and ethanol (70 ml) containing hydroxyamine hydrochloride (22.8 g) and diisopropylethylamine (34 ml), and thereafter, the reaction solution was stirred at room temperature for 67 hours, at 60° C. for 5 hours, and again, at room temperature for 20 hours. Thereafter, the generated solid was collected, and it was washed with ethanol (30 ml) and was then dried, so as to obtain the title compound (11.3 g) in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440970B2
Source datasetuspto-grants-2016_09
ORD IDord-40048a9e96304c19886aee2f1c61a747
Source noteuspto-grants-2016_09