Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642484Generated: November 1, 2026

1,1'-Carbonyldiimidazole → HCID 25221225, compound

https://huagongshe.com/reaction/1642484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantEthyl 3-[4-[[(1S,2S)-2-aminocyclohexyl]amino]-1-piperidinyl]-3-methyl-1-pyrrolidinecarboxylateHCID 57619822—
SolventAcetonitrileHCID 6342—
ProductHCID 25221225HCID 252212257%

Reaction Steps

A solution of ethyl 3-[4-[[(1S,2S)-2-aminocyclohexyl]amino]-1-piperidyl]-3-methyl-pyrrolidine-1-carboxylate (600 mg, 1.70 mmol) in anhydrous acetonitrile (30 mL) was added with 1,1′-carbonyldiimidazole (551.92 mg, 3.40 mmol) and stirred at room temperature for 12 h. The solvent was removed in vacuo; the residue was dissolved in dichloromethane (60 mL), washed with water and brine and dried over anhydrous MgSO4. Concentrated in vacuo and the residue was purified by flash chromatography (dichloromethane/methanol) to afford the title compound as a white solid (45 mg). 1H NMR (CD3OD, 400 MHz): δ 4.15 (q, 2H), 3.62-3.51 (m, 2H), 2.41 (m, 2H), 3.22 (m, 1H), 3.19 (brd, 1H), 2.99 (m, 3H), 2.76 (brs, 1H), 2.45 (m, 3H), 2.01-1.82 (m, 6H), 1.74 (brd, 1H), 1.65 (brd, 1H), 1.45 (m, 4H), 1.25 (t, 3H), 1.12 (s, 3H). MS (M+1): 379.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119661B2
Source datasetuspto-grants-2012_02
ORD IDord-56231d6830b242468801ea9b79f482a0
Source noteuspto-grants-2012_02