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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604242Generated: 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/604242

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, 4.63 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 numberUS07910553B2
Source datasetuspto-grants-2011_03
ORD IDord-dff6521e87cb4ee9a2456ac56cd10a34
Source noteuspto-grants-2011_03