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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900917Generated: October 31, 2026

Acetone → HCID 23370048, compound

https://huagongshe.com/reaction/1900917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMethyl iodideHCID 6328—
ReactantAmmonium AcetateHCID 517165—
ReactantHCID 23370060HCID 23370060—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 23370048HCID 2337004857.7%

Reaction Steps

In a similar manner to Example 1, the product from step (d) (380 mg), iodomethane (2 ml) and acetone (40 ml) were reacted at ambient temperature and the product so obtained was reacted with ammonium acetate (800 mg), ethanol (40 ml) and dichloromethane (20 ml). This yielded an oily residue which was purified by column chromatography on silica eluting with 10% ethanol/dichloromethane to give ethyl N-[N-(4-amidinobenzoyl)carbamoyl]piperidin-4-ylmethoxyacetate (210 mg) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576334
Source datasetuspto-grants-1996_11
ORD IDord-85989030e2dd4a17a2b4421fa28ef8e4
Source noteuspto-grants-1996_11