Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537136Generated: October 28, 2026

7-Bromo-1-Chloroisoquinoline → 7-Bromo-1-methoxyisoquinoline

https://huagongshe.com/reaction/537136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Bromo-1-ChloroisoquinolineHCID 6502024—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product7-Bromo-1-methoxyisoquinolineHCID 6749161193%

Reaction Conditions

Temperature130 °C

Reaction Steps

7-Bromo-1-chloroisoquinoline (570 mg, 2.4 mmol) was combined with methanol (10 mL) and sodium methoxide (25 wt % in methanol, 1.5 mL, 24 mmol) in a microwave vial. The vial was sealed and heated to 130° C. for 3 hours in a microwave. The reaction was concentrated. The crude residue was taken up in ethyl acetate and washed with water and saturated aqueous sodium bicarbonate. The aqueous layer was extracted two times with hot ethyl acetate. The combined organics were dried over sodium sulfate, filtered, and concentrated to give the title compound (520 mg, 93%). +ESI (M+H+1) 240.0; 1H NMR (400 MHz, DMSO-d6, δ): 8.25-8.28 (m, 1H), 8.04 (d, J=5.9 Hz, 1H), 7.86-7.89 (m, 2H), 7.40 (dd, J=6.0, 0.9 Hz, 1H), 4.03 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859773B2
Source datasetuspto-grants-2014_10
ORD IDord-dea21a31665d4ae1a139ad5a651f73d6
Source noteuspto-grants-2014_10