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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386823Generated: October 25, 2026

Diisopropylethylamine → 4-amino-N-(6-chloropyridin-2-yl)-1,2,5-oxadiazole-3-carboxamide

https://huagongshe.com/reaction/386823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-6-chloropyridineHCID 206246—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Amino-1,2,5-oxadiazole-3-carboxylic acidHCID 547454—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
Product4-amino-N-(6-chloropyridin-2-yl)-1,2,5-oxadiazole-3-carboxamideHCID 58558321—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 4-amino-1,2,5-oxadiazole-3-carboxylic acid (0.4 g, 3.1 mmol) and 6-chloropyridin-2-amine (0.56 g, 4.3 mmol) in N,N-dimethylformamide (6.2 mL) was treated with N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (1.4 g, 3.7 mmol) followed by N,N-diisopropylethylamine (0.76 mL, 4.3 mmol) at 0° C. The reaction mixture was stirred at 25° C. for 2 h, poured into saturated NaHCO3 (50 mL) and extracted with ethyl acetate (100 mL). The organic layer was separated and washed with brine (25 mL), dried with sodium sulfate, filtered, and concentrated to a crude solid. The crude solid was washed with ethyl acetate and filtered. The filtrate was concentrated and purified on silica gel to give the desired product with some impurities. The impurities were removed by washing the solid with chloroform to yield the desired product (65 mg, 9%). LCMS for C8H7ClN5O2 (M+H)+: m/z=240.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372870B2
Source datasetuspto-grants-2013_02
ORD IDord-3ad2befdb2c94623a11e7ad300d452c2
Source noteuspto-grants-2013_02