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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521854Generated: November 2, 2026

Morpholine → HCID 52950345, compound

https://huagongshe.com/reaction/1521854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantPropylphosphonic anhydrideHCID 111923—
ReactantHCID 66578670HCID 66578670—
SolventTetrahydrofuranHCID 8028—
ProductHCID 52950345HCID 52950345—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 6-methoxy-1-phenyl-1,4-dihydrothiochromeno[4,3-c]pyrazole-3-carboxylic acid 5,5-dioxide (0.20 g, 0.54 mmol) in THF (20 mL) is added triethylamine (0.20 mL, 1.63 mmol) followed by 50% propane phosphonic acid anhydride in EtOAc (0.70 mL, 0.347 g, 1.09 mmol). The reaction mixture is cooled to 0° C. and then morpholine (0.049 g, 0.59 mmol) is added and the reaction mixture is stirred overnight at room temperature. The solvent is removed under reduced pressure and the residue is diluted with EtOAc. The organic layer is washed with 10% NaHCO3 then brine, dried over MgSO4 and concentrated under reduced pressure. The residue is purified by column chromatography (eluent 1 to 2% MeOH in DCM) to afford the title compound as an off-white solid. 1H NMR (DMSO-d6, 400 MHz): δ 7.59-7.58 (m, 3H) 7.46-7.42 (m, 3H) 7.25 (d, J=8.60 Hz, 1H), 6.35 (d, J=7.92 Hz, 1H), 4.82 (s, 2H), 3.95 (br, 2H), 3.90 (s, 3H), 3.65 (br, 4H), 3.59 (br, 2H). MS (ESI+): 440.0. HPLC (max plot) 96.0%; Rt 4.81 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073940B2
Source datasetuspto-grants-2015_07
ORD IDord-90ca023542d54f468a41147985a300cd
Source noteuspto-grants-2015_07