HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 23370048, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 23370060 | HCID 23370060 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23370048 | HCID 23370048 | 57.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05576334 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-85989030e2dd4a17a2b4421fa28ef8e4 |
| Source note | uspto-grants-1996_11 |