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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362486Generated: October 26, 2026

L-Valine → N-(1,3-Dimethylindole-2-Carbonyl)Valine

https://huagongshe.com/reaction/362486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-ValineHCID 6287—
ReactantDichloromethaneHCID 6344—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1,3-dimethyl-1H-indole-2-carboxylic acidHCID 12496663—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductN-(1,3-Dimethylindole-2-Carbonyl)ValineHCID 5363759294.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

DMAP (367 mg, 3.0 mmol) and EDAC (748 mg, 3.9 mmol) were added as solids to a solution of 1,3-dimethylindole-2-carboxylic acid (568 mg, 3.3 mmol) in DMF (5 mL), and the resultant mixture was stirred for 10 minutes under a nitrogen atmosphere at 0° C. A methylene chloride solution of the methyl ester of valine (553 mg, 3.3 mmol, in 5 mL of methylene chloride) was added to the mixture, and the mixture was first stirred for one hour at 0° C. then for 5 hours at room temperature. The reaction mixture was partitioned between ethyl acetate and 5% KHSO4 solution and the aqueous solution was back-extracted with ethyl acetate. The combined ethyl acetate washes were in turn washed with 5% KHSO4 solution saturated sodium bicarbonate solution (2×) and brine, dried over sodium sulfate, and concentrated to give the title product as a yellow syrup (900 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869519
Source datasetuspto-grants-1999_02
ORD IDord-2390a3a8a36d45e9b8eaecc4a5edc2bf
Source noteuspto-grants-1999_02