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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835458Generated: October 30, 2026

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → N-[3-(pyrimidin-5-yl)-phenyl]-3-methyl-2-trifluoromethyl-1H-indole-7-carboxamide

https://huagongshe.com/reaction/1835458

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Pyrimidin-5-ylanilineHCID 7162049—
Reactant2-Trifluoromethyl-3-methylindole-7-carboxylic acidHCID 23503688—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-[3-(pyrimidin-5-yl)-phenyl]-3-methyl-2-trifluoromethyl-1H-indole-7-carboxamideHCID 2350364853.5%

Reaction Steps

To a suspension of 2-trifluoromethyl-3-methylindole-7-carboxylic acid (122 mg) and 3-(pyrimidin-5-yl)aniline (86 mg) in dichloromethane (3 ml) were added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (144 mg) and 4-dimethylaminopyridine (30 mg). The mixture was stirred at ambient temperature for 18 hours and diluted with dichloromethane. The solution was washed with water and brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by a silica gel column chromatography eluting with 2% methanol in dichloromethane to give N-[3-(pyrimidin-5-yl)-phenyl]-3-methyl-2-trifluoromethyl-1H-indole-7-carboxamide (106 mg, 53.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770667B1
Source datasetuspto-grants-2004_08
ORD IDord-edf6ec57a3bc41ef8757f7ad9bb1f8bf
Source noteuspto-grants-2004_08