Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463343Generated: November 1, 2026

Hydrochloric Acid → HCID 19921693, compound

https://huagongshe.com/reaction/1463343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzylamineHCID 7504—
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
ReactantHCID 19921669HCID 19921669—
SolventAcetonitrileHCID 6342—
ProductHCID 19921693HCID 1992169337%
ProductDichloromethane methanol ammonium hydroxideHCID 21896990—

Reaction Steps

To a mixture of 3-(3-hydroxypropyl)-1H-indole-5-carboxylic acid (4.30 g, 19.63 mmol), triethylamine (3.97 g, 39.26 mmol) and benzylamine (2.10 g, 19.63 mmol) in 150 mL acetonitrile was added 2-chloro-1-methylpyridinium iodide (6.04 g, 23.68 mmol). The mixture was heated to reflux for 16 h. The solution was cooled to room temperature, 70 mL of 0.5N hydrochloric acid added, and the acetonitrile removed in vacuo. The residue was extracted with 250 mL of ethyl acetate. The organic layer was separated and the aqueous layer reextracted with three 50 mL portions of ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. Silica gel chromatography (95:5:0.5 CH2Cl2 -MeOH-NH4OH) of the concentrate yielded 3-(3-hydroxypropyl)-N-(phenylmethyl)-1H-indole-5-carboxamide (2.26 g, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05300506
Source datasetuspto-grants-1994_04
ORD IDord-b317b5c1c9dc4cd280e061e47d28bf34
Source noteuspto-grants-1994_04