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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164881Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 54191163, compound

https://huagongshe.com/reaction/2164881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
ReactantN-Boc-L-Leucine HydrateHCID 12373896—
SolventEthyl AcetateHCID 8857—
ProductHCID 54191163HCID 5419116385.6%

Reaction Steps

Under cooling with ice, an ethyl acetate solution (40 ml) of N,N'-dicyclohexylcarbodiimide (10.3 g) was added dropwise to an ethyl acetate solution (150 ml) containing tert-butoxycarbonyl-L-leucine monohydrate (12.5 g) and N-hydroxy succinimide (5.76 g), and the mixture was stirred at room temperature for 3 hours. While cooling again with ice, 1-(2-pyridyl)piperazine (8.16 g) was added, and the mixture was stirred overnight at room temperature. The precipitate was removed by filtration, and the filtrate was washed first with an aqueous sodium carbonate solution and then with a saturated sodium chloride solution, dried over sodium sulfate and distilled under reduced pressure to remove the solvent, whereupon a crude reaction mixture was obtained. The reaction mixture was purified by silica gel column chromatography (developing solvent: methylene chloride:methanol=10:1) to yield 16.1 g of tert-butyl (s)-3-methyl-1-[4-(2-pyridyl)piperazine-1-yl carbonyl]butylcarbamate (yield: 85.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04507297
Source datasetuspto-grants-1985_03
ORD IDord-f648f5cc6765468e8fc2c5c6666c90b7
Source noteuspto-grants-1985_03