Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489895Generated: October 31, 2026

Morpholine → CP-640186

https://huagongshe.com/reaction/489895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 23589106HCID 23589106—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductCP-640186HCID 449097—

Reaction Steps

The crude (3R)-1′-(anthracene-9-carbonyl)-[1,4′]bipiperidinyl-3-carboxylic acid as prepared above (approx 22 mmol) was heated under reflux in a mixture of chloroform (75 mL, Aldrich, amylenes-stabilized) and thionyl chloride (10 mL, 0.137 mmol) until all the solid had dissolved. The mixture was diluted with toluene, evaporated to dryness under vacuum and anhydrous dichloromethane (40 mL) added. A mixture of morpholine (21 mmol, 1.81 mL) and triethylamine (62 mmol, 8.7 mL) in anhydrous dichloromethane (40 mL) was added and the solution was stirred for 16 hr at ambient temperature. The mixture was washed with ice-cold 0.1M sodium hydroxide solution, dried over anhydrous sodium sulfate, diluted with toluene and evaporated to dryness. The residue was purified by chromatography on 240 g silica gel eluting with a 4%-7%-10% methanol-dichloromethane gradient to give the title compound as a pale yellow glassy foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979741B2
Source datasetuspto-grants-2005_12
ORD IDord-b2a8817c47a14cb79288ce6ca561af77
Source noteuspto-grants-2005_12