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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908937Generated: October 25, 2026

4-Methylmorpholine → 2-(4-Dimethylamino-4-phenylcyclohexylidene)-N-[3-(1H-indol-3-yl)propyl]acetamide

https://huagongshe.com/reaction/908937

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantSodium HydroxideHCID 14798—
Reactant1H-indole-3-propylamineHCID 28989—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(4-Dimethylamino-4-phenylcyclohexylidene)acetic acid hydrochlorideHCID 67386703—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(4-Dimethylamino-4-phenylcyclohexylidene)-N-[3-(1H-indol-3-yl)propyl]acetamideHCID 1165535760%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Hydroxybenzotriazole (819 mg, 6.0 mmol), 3-(1H-indol-3-yl)propylamine (522 mg, 3.0 mmol) and N-methylmorpholine (0.666 ml, 6.0 mmol) were added to a solution of (4-dimethylamino-4-phenylcyclohexylidene)acetic acid hydrochloride (887 mg, 3.0 mmol) in dry dimethylformamide (10 ml) under argon. The solution was cooled to 0° C. and dicyclohexylcarbodiimide (1.25 g, 6.0 mmol) was added. The reaction mixture was stirred at RT for 6 d. Working up of the mixture was carried out by separating off the urea which had precipitated out and introducing the filtrate into a mixture of saturated NaCl solution (40 ml) and saturated NaHCO3 solution (10 ml). Still further urea thereby precipitated out and was separated off. The aqueous phase was diluted with water (400 ml), 5 M sodium hydroxide solution (5 ml, 25 mmol) was added and the mixture was stored at 5° C. for 3 d. The product thereby precipitated out as a beige-coloured solid in a yield of 60% (742 mg) with an m.p. of 85-87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017630B2
Source datasetuspto-grants-2011_09
ORD IDord-abc4871d7af74b08804964c15cf9de0e
Source noteuspto-grants-2011_09