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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777937Generated: October 31, 2026

(+-)-3-Quinuclidinol → Racemic 6-amino-4-(quinuclidin-3-yloxy)nicotinonitrile

https://huagongshe.com/reaction/1777937

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-3-QuinuclidinolHCID 15381—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant6-Amino-4-fluoronicotinonitrileHCID 118036901—
SolventTetrahydrofuranHCID 8028—
ProductRacemic 6-amino-4-(quinuclidin-3-yloxy)nicotinonitrileHCID 118036915—

Reaction Steps

A solution of KHMDS in THF (1 M, 6.6 ml, 6.60 mmol) was added drop wise to a solution of racemic quinuclidin-3-ol (928 mg, 7.29 mmol) in THF (2 ml) at room temperature. After 55 min a solution of 6-amino-4-fluoronicotinonitrile (intermediate 21, 500 mg, 3.65 mmol) in THF (2 ml) was added and the reaction mixture stirred for 3 days at room temperature. The reaction mixture was partitioned between saturated aqueous NH4Cl and DCM, extracted with DCM (8×), the combined DCM layers were dried over Na2SO4 and evaporated. The residue was preabsorbed onto silica gel and purified by normal phase chromatography with a 12 g RediSep® silica column, eluting with a gradient from DCM to 20% MeOH in DCM. Product containing fractions were combined and evaporated to give the title compound as a beige solid. (UPLC-MS 6) tR 0.32; ESI-MS 245.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266883B2
Source datasetuspto-grants-2016_02
ORD IDord-e6ece83d85674a7784aaef12ea1a3f0a
Source noteuspto-grants-2016_02