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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226614Generated: November 1, 2026

Diisopropylethylamine → (S)-1-(tert-Butyloxycarbonyl)-4-(dipentylcarbamoyl)piperazine-2-carboxylic acid

https://huagongshe.com/reaction/2226614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantDipentylcarbamyl chlorideHCID 22106956—
Reactant(2S)-1-[(tert-butoxy)carbonyl]piperazine-2-carboxylic acidHCID 40419053—
SolventDimethylformamideHCID 6228—
Product(S)-1-(tert-Butyloxycarbonyl)-4-(dipentylcarbamoyl)piperazine-2-carboxylic acidHCID 53820654—

Reaction Steps

A partial solution of 1.32 g (5.74 mmole) of (S)-1-(tert-butyloxycarbonyl)piperazine-2-carboxylic acid in 25 ml of dried DMF was treated dropwise over 5 min with 1.48 g (11.47 mmole of diisopropylethyl amine at 25° under nitrogen with stirring. The clear solution which resulted was treated dropwise over 15 min with a solution of 1.26 g (5.74 mmole) of dipentylcarbamoyl chloride in 5 ml of DMF and the mixture was stirred under nitrogen at 25° for 16 hr. The solution was concentrated in vacuo and the residue was dissolved in 100 ml of dichloromethane which was extracted with 2×100 ml of 0.5M citric acid and 2×25 ml of water. Without drying, the solution was concentrated in vacuo to 1.85g (78%) of medium yellow oil which was homogeneous by the (silica gel, 1:1:1:1 ethylacetate: n-butanol: acetic acid: water, Rf =0.50).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348955
Source datasetuspto-grants-1994_09
ORD IDord-699c6f02937442eda9dbc481a36c069f
Source noteuspto-grants-1994_09