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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277132Generated: November 2, 2026

Diisopropylethylamine → 2-(4-(Cyclopropylmethoxy)-3-fluorophenyl)-1,3-benzoxazol-6-ol

https://huagongshe.com/reaction/2277132

Reaction equation

Participants

RoleNameHCIDCharge
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—
Reactant4-Aminobenzene-1,3-diol hydrochlorideHCID 13408822—
Reactant4-(Cyclopropylmethoxy)-3-fluorobenzoic acidHCID 28604704—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-(4-(Cyclopropylmethoxy)-3-fluorophenyl)-1,3-benzoxazol-6-olHCID 8673118726.5%

Reaction Steps

To a solution of 4-aminoresorcinol hydrochloride (5.00 g), 4-(cyclopropylmethoxy)-3-fluorobenzoic acid (5.91 g) and diisopropylethylamine (7.37 mL) in DMF (50 mL) was added HATU (11.8 g), and the mixture was stirred at room temperature for 1 hr. The reaction mixture was diluted with ethyl acetate, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained solid was washed with ethyl acetate. To a solution of the obtained solid, hexachloroethane (16.7 g) and triphenylphosphine (18.5 g) in acetonitrile (50 mL) was added triethylamine (11.8 mL), and the mixture was stirred at room temperature for 15 min, and then with heating at 80° C. for 2 hr. The reaction mixture was filtered, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (2.23 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-5d5ee0b1e0f6462991cabfedcf847fbe
Source noteuspto-grants-2015_09