Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azetidine | HCID 10422 | — |
| Reactant | HCID 86721447 | HCID 86721447 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86721448 | HCID 86721448 | 99% |
Reaction Steps
[step 4] (E)-2-{8-[(4-chloro-2-methyl-6-propylpyrimidin-5-yl)methyl]-3-fluorodibenzo[b,e]oxepin-11(6H)-ylidene}propanenitrile (140 mg, 3.13 mmol) obtained in step 3 was dissolved in ethanol (3 mL), azetidine (0.148 mL, 2.19 mmol) was added, and the mixture was stirred with heating at 50° C. for 2 hr. The mixture was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/2 v/v) to give the title compound (145 mg, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969345B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-f9ace674d4c549528a3ef8aafc2f543d |
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| Source note | uspto-grants-2015_03 |
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