Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492182Generated: October 29, 2026

Lithium hydroxide, monohydrate → 1-(Isoquinolin-1-yl)-5-methyl-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/492182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantMethyl 1-(isoquinolin-1-yl)-5-methyl-1H-indole-3-carboxylateHCID 68968694—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(Isoquinolin-1-yl)-5-methyl-1H-indole-3-carboxylic acidHCID 6897140287.3%

Reaction Steps

0.319 g (7.59 mmol) of lithium hydroxide monohydrate and 60 cm3 of water are added at 25° C. to 1.2 g (3.79 mmol) of 3-methoxycarbonyl-1-(isoquinol-1-yl)-5-methyl-1H-indole dissolved in 60 cm3 of tetrahydrofuran. After stirring at the reflux point of the solvent for 24 hours, the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) to give a residue which is taken up in 30 cm3 of water and then triturated with 11.4 cm3 of N hydrochloric acid. After filtering off and drying the solid residue under reduced pressure (2.7 kPa) at 40° C., 1 g of 3-carboxy-1-(isoquinol-1-yl)-5-methyl-1H-indole is obtained in the form of a white solid. Mass spectrum (EI): m/e 302 (M+·), m/e 257.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531663B2
Source datasetuspto-grants-2009_05
ORD IDord-3eacb8f5cb8541c3a9cb131f1b489cad
Source noteuspto-grants-2009_05