HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178517968, compound → HCID 178507564, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178517968 | HCID 178517968 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178507564 | HCID 178507564 | — |
Reaction Steps
A 100 mL EtOH solution of 1.0 g (2.1 mmol) 8-(3-nitrobenzyl)-4-(cyclohexylamino)-1-(3-fluorophenyl)-1,3,8-triazaspiro[4.5]dec-3-en-2-one (example 104) and 0.57 g (2.5 mmol) SnCl2 dihydrate was heated to reflux and allowed to stir overnight. HPLC/MS showed complete conversion so the reaction mixture was filtered through celite washed with EtOH then the filtrate was concentrated. The remaining oil was partitioned between 3N NaOH and EtOAc. A thick white precipitate formed in the aqueous layer. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated to pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08114887B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-057ccbe7477f436583e6e7cc9963e9f8 |
| Source note | uspto-grants-2012_02 |