Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521571Generated: October 26, 2026

Oxalyl chloride → (S)-3-methyl-6-(methyl(1-phenylethyl)amino)-[1,2,4]triazolo[4,3-b]pyridazine-8-carboxamide

https://huagongshe.com/reaction/521571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantAmmonia tetrahydrofuranHCID 21982362—
Reactant(S)-3-methyl-6-(methyl(1-phenylethyl)amino)-[1,2,4]triazolo[4,3-b]pyridazine-8-carboxylic acidHCID 71115949—
SolventTetrahydrofuranHCID 8028—
Product(S)-3-methyl-6-(methyl(1-phenylethyl)amino)-[1,2,4]triazolo[4,3-b]pyridazine-8-carboxamideHCID 7111601190%

Reaction Steps

To a solution of compound (S)-3-methyl-6-(methyl(1-phenylethyl)amino)-[1,2,4]triazolo[4,3-b]pyridazine-8-carboxylic acid (200 mg, 0.64 mmol) in anhydrous THF (10 mL) was added oxalyl chloride (0.3 mL) dropwise. The reaction mixture was stirred at room temperature for 2 hrs, then 2N NH3/THF (1 mL) solution was added, and stirred for another 2 hrs. The mixture was concentrated in vacuum and the residue was purified by flash column chromatography (silica-gel, DCM: MeOH=20:1) to give product (S)-3-methyl-6-(methyl(1-phenylethyl)amino)-[1,2,4]triazolo[4,3-b]pyridazine-8-carboxamide (Compound 7) as a yellow solid (180 mg, 90%). 1H NMR (300 MHz, DMSO) δ 8.66 (s, 1H), 8.40 (s, 1H), 7.66 (s, 1H), 7.26˜7.36 (m, 5H), 5.71˜5.74 (q, 1H), 2.90 (s, 3H), 2.59 (s, 3H), 1.61 (d, J=6.9 Hz, 3H). LRMS (M+H+) calcd. 310; found 310.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328117B2
Source datasetuspto-grants-2016_05
ORD IDord-f78ab00642284c2688c30bdd6f72331a
Source noteuspto-grants-2016_05