HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 7-chloro-6-oxoheptanoate → HCID 20202828, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 7-chloro-6-oxoheptanoate | HCID 15576276 | — |
| Reactant | HCID 178512206 | HCID 178512206 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20202828 | HCID 20202828 | — |
Reaction Steps
To a solution of methyl 7-chloro-6-oxoheptanoate (2.0 g.) in hot EtOH (20 ml.) was added a solution of 2,2,2-trifluoroethylamidinothiourea (2.1 g.) in hot EtOH (20 ml.). The resulting mixture was heated under reflux for 1 hour. The mixture was then evaporated to dryness and the residue partitioned between ether (20 ml.) and water (60 ml.). The aqueous layer was separated and basified with sodium bicarbonate and extracted with EtOAc. The EtOAc solution was evaporated to dryness and the residue crystallised from EtOAc/ether containing a small amount of acetone to give methyl 5-[2-(2-[2,2,2-trifluoroethyl]guanidino)thiazol-4-yl]valerate which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04447441 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-f4f84448db5c48d2889f6ef096580f2c |
| Source note | uspto-grants-1984_05 |