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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521835Generated: October 30, 2026

Morpholine → HCID 66579017, compound

https://huagongshe.com/reaction/1521835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantPropylphosphonic anhydrideHCID 111923—
ReactantHCID 66578972HCID 66578972—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66579017HCID 6657901777.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 1-methyl-8-nitro-1,4-dihydrothiochromeno[4,3-c]pyrazole-3-carboxylic acid (0.088 g, 0.30 mmol) in THF is added triethylamine (0.13 mL, 0.9 mmol, 3 Eq) followed by 50% T3P (propane phosphonic acid anhydride) in EtOAc (0.50 mL, 0.81 mmol, 2.7 Eq). The reaction mixture is cooled to 0° C. and then morpholine (0.38 mL, 0.60 mmol, 2Eq) is added and the reaction is stirred overnight at rt. Then the solvent is removed under vacuo and the residue is diluted with EtOAc. The organic layer is washed with 10% NaHCO3 followed by brine. The organic layer is dried over MgS)4and concentrated in vacuo to afford 0.084 g (77%) of the title compound as a white solid. 1H NMR (DMSO-d6, 400 MHz) δ 8.55 (d, J=2.4 Hz, 1H), 8.10 (dd, J=8.5 Hz, J=2.4 Hz, 1H), 7.76 (d, J=8.7 Hz, 1H), 4.20 (s, 3H), 4.19 (s, 2H), 3.95 (brs, 2H), 3.63 (brs, 6H). MS (ESI+): 359.0. HPLC (max plot) 96.9%; Rt 3.78 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073940B2
Source datasetuspto-grants-2015_07
ORD IDord-4de395e617bc45ca8fe4953eea7b2c90
Source noteuspto-grants-2015_07