Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394241Generated: October 31, 2026

4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride → 5-(1h-Indol-3-yl)pentanoic acid [(4-dimethylamino-4-phenylcyclohexylcarbamoyl)-methyl]amide

https://huagongshe.com/reaction/1394241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
Reactant2-(1H-indol-3-yl)pentanoic acidHCID 23023001—
Reactant2-Amino-n-(4-dimethylamino-4-phenylcyclohexyl)acetamideHCID 69216915—
SolventMethanolHCID 887—
Product5-(1h-Indol-3-yl)pentanoic acid [(4-dimethylamino-4-phenylcyclohexylcarbamoyl)-methyl]amideHCID 12986257—

Reaction Steps

The more polar diastereomer of 2-amino-N-(4-dimethylamino-4-phenylcyclohexyl)-acetamide (159 mg, 0.57 mmole) and 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (239 mg, 0.86 mmole) were added to a solution of indol-3-yl-pentanoic acid (125 mg, 0.57 mmole) in MeOH and stirred for 24 h at room temperature. Working up was performed by removing MeOH by distillation. The batch was re-dissolved with water, adjusted to pH 11 with 5M NaOH and extracted with ethyl acetate. The organic phase was dried with Na2SO4 and evaporated. The more polar amide was obtained as a colorless oil in a yield of 273 mg (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348354B2
Source datasetuspto-grants-2008_03
ORD IDord-28b361eb4eeb4ee9a9be4c423dc71435
Source noteuspto-grants-2008_03