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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349936Generated: October 30, 2026

(S)-[(2R,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanol → HCID 131726431, compound

https://huagongshe.com/reaction/1349936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-[(2R,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanolHCID 5953—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBoc-L-ValineHCID 83693—
ReactantDichloromethane methanolHCID 21226129—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 131726431HCID 131726431—

Reaction Conditions

Temperature0 °C

Reaction Steps

Boc-Val-OH (2.00 g., 9.26 mmol) and DCC (1.90 g, 9.26 mmol) were dissolved in dry DMF (20 ml) under a nitrogen atmosphere. The mixture was stirred continuously for one hour at 0° C. A solution of quinidine (1.50 g, m4.63 mmol)) and DMAP (0.06 g, −0.65 mmol) in DMF (100 ml) was added dropwise to the reaction mixture at 0° C. The reaction mixture was stirred and allowed to warm to room temperature. After 24 hours, the reaction was checked by TLC (1:13 methanol/dichloromethane mixture) and LC-MS analysis, and was found to be complete. The urea derivative was removed by filtration and washed with ethyl acetate. Solvents from the combined filtrate and washing were totally removed under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214664B2
Source datasetuspto-grants-2007_05
ORD IDord-942a32a486e44560b1c0f1fb73325e74
Source noteuspto-grants-2007_05