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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299112Generated: October 29, 2026

Hydrochloric Acid → 1-[(2-methyl-5,8-dihydro-4-quinolinyl)methyl]-1H-indole-5-carboxylic acid

https://huagongshe.com/reaction/2299112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant1H-Indole-5-Carboxylic AcidHCID 74280—
Reactant4-(Chloromethyl)-2-methylquinolineHCID 11535719—
SolventDimethylformamideHCID 6228—
Product1-[(2-methyl-5,8-dihydro-4-quinolinyl)methyl]-1H-indole-5-carboxylic acidHCID 2225869869%

Reaction Conditions

Temperature0 °C

Reaction Steps

Indole 5-carboxylic acid (0.5 g, 3.1 mmol) was added to a suspension of sodium hydride (0.27 g, 6.8 mmol, 60% oil dispersion) (washed with hexanes) in DMF (20 ml) cooled to 0° C. The reaction was allowed to stir for 1 h and the 4-chloromethyl-2methyl-quinoline (0.72 g, 3.8 mmol) was added. The reaction was allowed to warm to room temperature and stir overnight. The reaction was neutralized with 1 N HCl and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over magnesium sulfate and concentrated to give the 1-[(2-methyl-5,8-dihydro-4-quinolinyl)methyl]-1H-indole-5-carboxylic acid (0.68 g, 69%) as a brown residue, MS (M+H)+=317.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495565B2
Source datasetuspto-grants-2002_12
ORD IDord-fa676cf38cec463989cccb8c1cf3a8a1
Source noteuspto-grants-2002_12