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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893458Generated: October 31, 2026

Triphenylphosphine → HCID 59333330, compound

https://huagongshe.com/reaction/1893458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Morpholinecarbonyl chlorideHCID 84810—
ReactantHCID 59333289HCID 59333289—
CatalystCopper iodideHCID 83717—
SolventTriethylamineHCID 8471—
ProductHCID 59333330HCID 5933333030%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-ethynyl-N-[3-(tetrahydro-2H-pyran-2-yloxy)propyl]-7-(trifluoromethyl)imidazo [1,2-a]quinoxalin-4-amine (46 mg, 0.11 mmol), copper iodide (1 mg, 0.0055 mmol), triphenylphosphine (3 mg, 0.11 mmol) and Pd(PPh3)Cl2 (1.5 mg, 0.0022 mmol) in anhydrous triethylamine (0.5 mL) was added morpholine-4-carbonyl chloride (17 μL, 0.16 mmol) under an argon atmosphere. The mixture was stirred at 80° C. for 40 h, poured onto water and extracted four times with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered and evaporated. The crude product was purified by preparative TLC (silica gel, dichloromethane/methanol 20/1) to afford the title compound (17 mg, 30%) as a yellow gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513250B2
Source datasetuspto-grants-2013_08
ORD IDord-c941597d311642fd99366d8a49408e5d
Source noteuspto-grants-2013_08