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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296780Generated: October 26, 2026

6-Aminoquinoline → n-(6-Quinolinyl)quinuclidine-3-carboxamide hydrochloride

https://huagongshe.com/reaction/1296780

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-AminoquinolineHCID 11373—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Quinuclidinecarbonyl chloride HydrochlorideHCID 12673437—
SolventDimethylformamideHCID 6228—
Productn-(6-Quinolinyl)quinuclidine-3-carboxamide hydrochlorideHCID 10149725—

Reaction Steps

172 mg (1.19 mmol) of 6-aminoquinoline are mixed with 461 mg (3.57 mmol) of N,N-diisopropylethylamine in 3 ml of DMF under argon at 0° C. 250 mg (2.57 mmol) of 3-quinuclidinecarbonyl chloride hydrochloride are dissolved in a little dry DMF and added dropwise to the reaction mixture at 0° C. It is then stirred at room temperature overnight. It is worked up by concentrating and taking up in dichloromethane. The crude product is chromatographed on silica gel 60 (mobile phase: dichloromethane/ethyl acetate 10:1, then dichloromethane/methanol 10:1, 3:1). The product fractions are combined and finally purified by preparative HPLC (RP18 column; mobile phase: acetonitrile/water, gradient 1:99→30:70).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247728B2
Source datasetuspto-grants-2007_07
ORD IDord-fc776fb3e8584746a568e2d06187f522
Source noteuspto-grants-2007_07