Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 86610913 | HCID 86610913 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 86610914 | HCID 86610914 | — |
Reaction Steps
In a pressure tube, 22 mg (0.0394 mmol) 3-[(3R,4S)-3-({(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethyl}oxy)-4-(4-fluorophenyl)pyrrolidin-1-yl]-2-[(dimethylamino)methyl]cyclopent-2-en-1-one (step A), and 0.025 mL (0.3939 mmol) iodomethane was dissolved in benzene (1 mL). The tube was sealed and heated in an oil bath for 2.5 hr at ˜60° C. The reaction mixture was cooled to RT, the tube was opened and the solvent removed under vacuum to afford the title compound as a yellow oil which was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468437B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-d27cedab06644149977ff396e8d5dc0b |
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| Source note | uspto-grants-2008_12 |
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