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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4,6-Dichloropyrimidine | HCID 70943 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 6-Hydroxyisoquinoline-1-carboxylic acid | HCID 136304046 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(6-Chloropyrimidin-4-yloxy)isoquinoline-1-carboxylic acid | HCID 86638623 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08133886B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-7f157121284f4e48bed72aeedcf010e6 |
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| Source note | uspto-grants-2012_03 |
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