Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091303Generated: October 30, 2026

Tetrahydrofuran → 4-{[1-(5-chloro-1-methyl-1H-indol-2-yl)heptyl]amino}benzoic acid

https://huagongshe.com/reaction/2091303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactantmethyl 4-{[1-(5-chloro-1-methyl-1H-indol-2-yl)heptyl]amino}benzoateHCID 66778860—
SolventEthanolHCID 702—
Product4-{[1-(5-chloro-1-methyl-1H-indol-2-yl)heptyl]amino}benzoic acidHCID 6677781298.1%

Reaction Steps

To a mixture of methyl 4-{[1-(5-chloro-1-methyl-1H-indol-2-yl)heptyl]amino}benzoate (1.15 g) synthesized above, tetrahydrofuran (15 mL) and ethanol (15 mL) was added 1N is aqueous sodium hydroxide solution (15 mL), and the mixture was stirred overnight with heating under reflux, and concentrated under reduced pressure. The residue was dissolved in water (30 mL), and 1N hydrochloric acid (15 mL) was added at 0° C. The resulting precipitate was collected by filtration to give the title object compound (1.09 g, 98%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-a55f51df099949dda6fe05c4c2107db9
Source noteuspto-grants-2013_05