Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245286Generated: October 30, 2026

Dicyclohexylcarbodiimide → 8-Fluoro-isoquinoline-3-carboxylic acid{(s)-1-azabicyclo[2.2.2]oct-2-yl}-amide

https://huagongshe.com/reaction/2245286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-quinuclidin-3-amineHCID 719216—
Reactant8-Fluoroisoquinoline-3-carboxylic acidHCID 68545393—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
Product8-Fluoro-isoquinoline-3-carboxylic acid{(s)-1-azabicyclo[2.2.2]oct-2-yl}-amideHCID 6855058835%

Reaction Steps

Dicyclohexyl-carbodiimide (7.69 g, 30 mmol) is added to a solution of 8-fluoro-isoquinoline-3-carboxylic acid (5.1 g, 22.4 mmol), ethyl-diisopropyl-amine (4.6 ml, 26.88 mmol) and hydroxybenzotriazole (5.36 g, 33.6 mmol) in DMF (150 ml). The mixture is stirred for 2 hours at room temperature. (S)-(1-Aza-bicyclo[2.2.2]oct-3-yl)amine (4.46 g, 49.28 mmol) and ethyl-diisopropyl-amine (8.7 ml, 49.28 mmol) are added and the solution is stirred for another 18 hours at room temperature. The solvent is removed by evaporation and the residue is dissolved in methylenedichloride and washed with a saturated K2CO3 solution and brine. The organic layer is dried over MgSO4 and evaporated. The crude product is purified by chromatography (CH2Cl2/MeOH/NH4OH, 92.5/7.5/0.75) to afford the desired compound (2.35 g). The product is recrystallized from ethanolic HCl to give 2 g. of the hydrochloric salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683075B2
Source datasetuspto-grants-2010_03
ORD IDord-71871602fe904859a754ca0db7e542e5
Source noteuspto-grants-2010_03