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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394239Generated: October 30, 2026

4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride → n-[(4-Dimethylamino-4-phenylcyclohexylcarbamoyl)methyl]-3-(1h-indol-3-yl)butyramide

https://huagongshe.com/reaction/1394239

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
Reactant2-(1H-indol-3-yl)butanoic acidHCID 12230080—
Reactant2-Amino-n-(4-dimethylamino-4-phenylcyclohexyl)acetamideHCID 69216915—
SolventMethanolHCID 887—
Productn-[(4-Dimethylamino-4-phenylcyclohexylcarbamoyl)methyl]-3-(1h-indol-3-yl)butyramideHCID 69216438—

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-butyric acid (117 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 265 mg (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348354B2
Source datasetuspto-grants-2008_03
ORD IDord-616b565f0e9a449c831041d0e3f0aac6
Source noteuspto-grants-2008_03