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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394243Generated: October 30, 2026

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

https://huagongshe.com/reaction/1394243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
Reactant2-Amino-n-(4-dimethylamino-4-phenylcyclohexyl)acetamideHCID 69216915—
ReactantIndol-3-yl-hexanoic acidHCID 69219720—
SolventMethanolHCID 887—
Product6-(1h-Indol-3-yl)hexanoic acid [(4-dimethylamino-4-phenylcyclohexylcarbamoyl)methyl]amideHCID 10481952—

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-hexanoic acid (133 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 281 mg (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348354B2
Source datasetuspto-grants-2008_03
ORD IDord-882cdf573f4049a0a0a1f7479cf95d9f
Source noteuspto-grants-2008_03