Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849881Generated: November 4, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 53638145, compound

https://huagongshe.com/reaction/849881

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
ReactantHCID 54555847HCID 54555847—
SolventDichloromethaneHCID 6344—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 53638145HCID 5363814575.4%

Reaction Steps

N-tert-Butyloxycarbonylpiperidin-4-carboxylic acid (97 mg; 0.424 mmol) was dissolved in methylene chloride (2 ml). HOAt (58 mg; 0.424 mmol) and EDAC (85 mg; 0.444 mmol) were added. The reaction mixture was stirred 15 min at RT. (2R)-2-Methylamino-3-(2-naphthyl)-N-((1R)-2-(2-naphthyl)-1-thiocarbamoylethyl)propionamide (17 mg; 0.386 mmol) was dissolved in methylene chloride (2 ml) and added. Diisopropylethylamine (0.073 ml; 0.424 mmol) was added and the reaction mixture was stirred 12 hours at room temperature. Tert-butylmethylether (25 ml) was added and the reaction mixture was washed with water (25 ml), aqueous sodium hydrogencarbonate (15 ml), aqueous sodiumhydrogensulfate (10%; 15 ml), water (15 ml) and dried (magnesium sulfate). The solvent was removed in vacuo and the residue was chromatographed on silica (3.5×30 cm) using gradient elution, starting with ethyl acetate/heptane (1:1) increasing to ethyl acetate/heptane (2:1) to afford 0.190 g of 4-(N-methyl-N-((1R)-2-(2-naphtyl)-1-((1R)-2-(2-naphthyl)-1-thiocarbamoylethylcarbamoyl)ethyl)carbamoyl)piperidine-1-carboxylic acid tert-butylester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06013658
Source datasetuspto-grants-2000_01
ORD IDord-884136114c21443a859b83c3778295cf
Source noteuspto-grants-2000_01