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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983916Generated: October 26, 2026

Sodium Carbonate → 4-(7-chloro-1H-indazol-5-yl)-isoquinoline

https://huagongshe.com/reaction/1983916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantIsoquinoline-4-boronic acidHCID 3761204—
Reactant5-Bromo-7-chloro-1H-indazoleHCID 21102194—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(7-chloro-1H-indazol-5-yl)-isoquinolineHCID 6899799672.1%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of isoquinolin-4-ylboronic acid (1.00 g, 5.78 mmol), 5-bromo-7-chloro-1H-indazole (892 mg, 3.85 mmol), 2.0 M sodium carbonate (3.85 mL, 7.71 mmol) and dimethoxyethane was degassed with argon. Tetrakis(triphenylphosphine)palladium(0) (233 mg, 0.193 mmol) was added, the mixture degassed again with argon, then heated to 85° C. for 24 hours. The reaction was cooled and partitioned between ethyl acetate and water, the organic layer washed with and dried with sodium sulfate. The solvent was removed under vacuum and the residue purified by column chromatography (9/1 to 6/4 hexanes/ethyl acetate gradient) to give 4-(7-chloro-1H-indazol-5-yl)-isoquinoline (777 mg, 72%): 1H NMR (300 MHz, CDCl3) δ 10.52 (s, 1H) 9.31 (s, 1H), 8.53 (s, 1H), 8.22 (s, 1H), 8.09 (dd, J=7.4, 1.62 Hz, 1H), 7.28 (dd, J=7.4, 1.2 Hz, 1H), 7.87 (d, J=9.0 Hz, 1H), 7.81 (d, J=1.2 Hz, 1H), 7.72-7.64 (m, 2H), 7.57 (d, J=1.3 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541357B2
Source datasetuspto-grants-2009_06
ORD IDord-ea7fe082ffb1421db7d7a299cff7e091
Source noteuspto-grants-2009_06