HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336557Generated: October 30, 2026
Potassium Hydroxide → HCID 68000203, compound
https://huagongshe.com/reaction/336557
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 131732013 | HCID 131732013 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | HCID 68000203 | HCID 68000203 | 95.8% |
Reaction Steps
0.726 g (12.95 mmol) of potassium hydroxide is added, at room temperature, to a solution of 0.242 g (0.65 mmol) of ethyl[7-(6-chloroquinolin-2-yl)-7-azaspiro[3.5]non-2-yl]carbamate, obtained in step 12.5., in 3.25 mL of ethanol/water (1/1). The mixture is then heated at 110° C. for 12 hours. 0.363 g (6.47 mmol) of potassium hydroxide is added and the mixture is left stirring for 3 hours. The resulting mixture is allowed to cool to room temperature and is then concentrated under reduced pressure. The residue is taken up in dichloromethane and 1N hydrochloric acid solution. The acidic aqueous phase is washed with dichloromethane and then basified with aqueous 1N sodium hydroxide solution, which is extracted several times with dichloromethane. The combined organic phases are then dried over sodium sulfate and the filtrate is concentrated under reduced pressure. 0.188 g of expected product is thus obtained in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08889702B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-db79ea0384814cb6a7396df9dd53d99d |
|---|
| Source note | uspto-grants-2014_11 |
|---|