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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878395Generated: November 4, 2026

Cyclobutylamine → HCID 57917682, compound

https://huagongshe.com/reaction/1878395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutylamineHCID 75645—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantHCID 57917599HCID 57917599—
SolventDichloromethaneHCID 6344—
ProductHCID 57917682HCID 5791768229.8%

Reaction Steps

To 3-((4-(4-amino-3-fluorobenzoyl)-2,2-dimethylpiperazin-1-yl)methyl)-N-tert-butylbenzamide (0.1 mmol, 45 mg) in dichloromethane (1.5 mL) was added 4-nitrophenyl chloroformate (0.11 mmol, 23 mg). The mixture was allowed to stir for 2 hours before the addition of cyclobutylamine (1.757 mmol, 125 mg, 150 μl). The mixture was allowed to stir for a further 16 hours before being concentrated under vacuum and purified by acidic reverse phase HPLC. The free base of the product was obtained using strong cation exchange column chromatography. This material was lyophilised to yield the title compound (16 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314091B2
Source datasetuspto-grants-2012_11
ORD IDord-4955a4a629734803982e719124a9a179
Source noteuspto-grants-2012_11