HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → HCID 59966108, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 53817166 | HCID 53817166 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59966108 | HCID 59966108 | 76% |
Reaction Steps
To a stirred solution of 1-[(R)-1-allyl-3-(1-methyl-2-pyrrolidinylmethyl)-1H-indol-5-yl]-1-cyano-N-diphenylmethyl-N-methylmethanesulfonamide (from step (b), 5.11 g, 9.25 mmol) in ethanol (10.22 ml) at ambient temperature was added 2N potassium hydroxide solution (20.4 ml, 41 mmmol). The dark brown solution was then brought to reflux and maintained at this temperature for 15 hr. The oily reaction mixture was then cooled to ambient temperature and extracted with ethyl acetate (3×50 ml). The organic extracts were combined and evaporated in vacuo to yield a dark brown oil. This was purified by flash column chromatography (ethyl acetate:hexane:diethylamine 1:1:0.1 as eluant) to yield the title compound (3.7 g, 76%) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06281357B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-1392c3e947bd491d9975f3a217ee31f5 |
| Source note | uspto-grants-2001_08 |