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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094525Generated: November 1, 2026

4,6-Dichloropyrimidine → 6-(6-Chloropyrimidin-4-yloxy)isoquinoline-1-carboxylic acid

https://huagongshe.com/reaction/1094525

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-DichloropyrimidineHCID 70943—
ReactantSodium MethoxideHCID 10942334—
Reactant6-Hydroxyisoquinoline-1-carboxylic acidHCID 136304046—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product6-(6-Chloropyrimidin-4-yloxy)isoquinoline-1-carboxylic acidHCID 86638623—

Reaction Conditions

Temperature10 °C

Reaction Steps

40 ml (20 mMol) of a 0.5 M solution of sodium methylate in MeOH are added to a suspension of 1.9 g (10 mMol) 6-hydroxy-isoquinoline-1-carboxylic acid (CAS 174299-07-1) in 50 ml MeOH and sonicated until a solution is obtained. The solvent is then evaporated off. The residue is dried in high vacuum for 4 h and 100 ml DMF are added. The suspension is cooled to 10° C. and a solution of 1.55 g (10 mMol) 4,6-dichloropyrimidine in 25 ml DMF is added. The reaction mixture is stirred at room temperature for 14 h. The solvent is evaporated off and the mixture is partitioned between H2O/EtOAc. After extraction, the aqueous phase is neutralized with a 1 N solution of HCl. The suspension is extracted with EtOAc, washed with H20 and brine, dried (MgSO4) and concentrated to give a beige powder: 1H-NMR (DMSO-d6): δ ppm 7.60 (s, 1H), 7.68 (dd, J=9.4, 2.3 Hz, 1H), 7.98 (d, J=2.3 Hz, 1H), 8.04 (d, J=5.5 Hz, 1H), 8.59 (d, J=5.9 Hz, 1H), 8.66 (s, 1H), 8.68 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133886B2
Source datasetuspto-grants-2012_03
ORD IDord-7f157121284f4e48bed72aeedcf010e6
Source noteuspto-grants-2012_03