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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340631Generated: October 26, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 86692009, compound

https://huagongshe.com/reaction/340631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(4-Bromophenyl)piperazineHCID 2735629—
Reactant2,2-Difluorocyclopropane-1-carboxylic acidHCID 2782823—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
SolventHeptaneHCID 8900—
ProductHCID 86692009HCID 86692009—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 1-(4-bromophenyl)piperazine (2.53 g, 10.5 mmol) in DMF (10 mL) was added 2,2-difluorocyclopropanecarboxylic acid (1.92 g, 15.7 mmol) 1H-benzotriazol-1-ol (2.84 g, 21.0 mmol), N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide (3.26 g, 21.0 mmol) and DIEA (7.31 mL, 42.0 mmol). The resulting mixture was stirred at 50° C. for 1 h. The reaction mixture was then quenched with saturated ammonium chloride solution, extracted with ethyl acetate, and concentrated in vacuo. Purification by chromatography on silica gel (0 to 75% EtOAc in hexanes, then 75 to 100% EtOAc in hexanes) provided the racemic compound. The racemate was then dissolved in 10% ethanol in heptane and the enantiomers were separated on an OD chiral column by eluting column with 30% ethanol in heptane. The first eluting peak was defined as enantiomer A and the second eluting peak was defined as enantiomer B. LCMS m/z 346.8 [M+H]+; 1H NMR (500 MHz, CD2Cl2) δ 7.37 (d, J=9.0 Hz, 2 H),6.80 (d, J=9.0 Hz, 2 H), 4.00-3.93 (m, 1 H),3.84-3.61 (m, 3 H),3.31-3.02 (m, 4 H),2.60-2.50 (m, 1 H),2.23-2.11 (m, 1 H),1.75-1.64 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895583B2
Source datasetuspto-grants-2014_11
ORD IDord-b0ee99ca52a14c3397a245bbd1b807a5
Source noteuspto-grants-2014_11