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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362477Generated: October 30, 2026

Dichloromethane → HCID 86583993, compound

https://huagongshe.com/reaction/362477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1H-Indole-2-carboxylic acid, 1-methyl-HCID 27695—
ReactantHCID 86583994HCID 86583994—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 86583993HCID 86583993—

Reaction Steps

1-Methylindole-2-carboxylic acid (88 mg, 0.5 mmol) and (3S)-3-(Valinyl)amino-4-oxobutanoic acid, t-butyl ester semicarbazone (163 mg, 0.5 mmol) were dissolved in DMF (1 mL) and methylene chloride (2 mL) then both DMAP (61 mg, 0.50 mmol) and EDAC (134 mg, 0.7 mmol) were added to the solution under a nitrogen atmosphere at 0° C. Stirring was continued for 1 hour at 0° C. and an additional 4 hours at room temperature. The reaction mixture was partitioned between ethyl acetate and 5% KHSO4 solution. The ethyl acetate solution was washed successively with 5% KHSO4 solution, saturated sodium bicarbonate solution and brine solutions, dried over sodium sulfate, and concentrated to give a yellow foam. Trituration of the foam with ether afforded the title product as a slightly yellow powder (203 mg, 86%). TLC: (methanol/methylene chloride:5/95, silica gel): Rf =0.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869519
Source datasetuspto-grants-1999_02
ORD IDord-3beef12bb64d416d8483fcdd9c10a299
Source noteuspto-grants-1999_02