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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370502Generated: November 1, 2026

2,3-Dihydro-1,4-benzodioxin-5-carboxylic acid → HCID 57725495, compound

https://huagongshe.com/reaction/2370502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydro-1,4-benzodioxin-5-carboxylic acidHCID 78184—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 24821873HCID 24821873—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 57725495HCID 57725495—

Reaction Conditions

Temperature40 °C

Reaction Steps

4-(2-Amino-benzooxazol-6-yloxy)-pyridine-2-carboxylic acid methylamide (1 eq) and 2,3-dihydro-1,4-benzodioxane-5-carboxylic acid (1 eq) were dissolved in DMF. To this solution were added DIPEA (3 eq) and [dimethylamino-([1,2,3]triazolo[4,5-b]pyridin-3-yloxy)-methylene]-dimethyl-ammonium hexafluoro phosphate (1 eq). The mixture was stirred at 40° C. overnight, then diluted with ethyl acetate and washed once each with 1N HCl, saturated aqueous sodium bicarbonate, and brine, and finally dried with anhydrous sodium sulfate, filtered, and concentrated. This was purified by preparatory reverse phase HPLC. MH+=447.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710048B2
Source datasetuspto-grants-2014_04
ORD IDord-22faf354bae74c198bf6ee99c8a35344
Source noteuspto-grants-2014_04