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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642477Generated: November 2, 2026

1,1'-Carbonyldiimidazole → HCID 57619816, compound

https://huagongshe.com/reaction/1642477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 57619817HCID 57619817—
SolventAcetonitrileHCID 6342—
ProductHCID 57619816HCID 5761981630%

Reaction Steps

A solution of tert-butyl 4-[4-[[(1R,2R)-2-aminocyclohexyl]amino]-1-piperidyl]-4-methyl-piperidine-1-carboxylate in acetonitrile (20 mL) was added with 1,1′-carbonyldiimidazole (1.30 g, 8.0 mmol) and the reaction mixture was stirred at room temperature for 12 h. The solvent was removed in vacuo and the residue was taken up in water (20 mL) and dichloromethane (80 mL). The phases were separated and the aqueous phase was extracted with dichloromethane (2×50 mL). The combined organic phases were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to give the crude product, which was purified with preparative LC/MS (high pH) to give the title compound as white solid (849 mg, 30% over two steps). 1H NMR (400 MHz, METHANOL-D4) δ ppm 0.95 (s, 3H), 1.31-1.40 (m, 4H), 1.42 (s, 9H), 1.44-1.48 (m, 2H), 1.52-1.63 (m, 1H), 1.64-1.89 (m, 8H), 1.93-1.99 (m, 1H), 2.08-2.21 (m, 2H), 2.25-2.32 (m, 1H), 2.89-3.10 (m, 4H), 3.28-3.36 (m, 1H), 3.42-3.53 (m, 2H), 3.54-3.65 (m, 1H). MS (M+1): 421.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119661B2
Source datasetuspto-grants-2012_02
ORD IDord-ce068dc63d634dd1958855b991e1b748
Source noteuspto-grants-2012_02