Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | HCID 178426061 | HCID 178426061 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178495758 | HCID 178495758 | 29.6% |
Reaction Steps
A mixture of trans-8-chloro-1-[4-(5-methyl-isoxazol-3-yl)-cyclohexyl]-5,6-dihydro-4H-2,3,5,10b-tetraaza-benzo[e]azulene (50 mg, 0.13 mmol), cesium carbonate (85 mg, 0.26 mmol) and 2-bromoethyl methyl ether (0.025 ml, 0.26 mmol) in acetonitrile (1.3 ml) was heated at 70° C. for 20 h. After cooling to room temperature the reaction mixture was partitioned between 1 M aqueous sodium hydroxide solution (2 ml) and ethyl acetate (5 ml). The layers were separated. The aqueous layer was extracted with three 5-ml portions of ethyl acetate. The combined organic layers were concentrated in vacuo. Preparative RP-HPLC with water (0.05% formic acid)/methanol as eluent gave the title compound (17 mg, 29%) as off-white solid. MS m/e: 442 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513238B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-e588216684884723855172038c22249c |
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| Source note | uspto-grants-2013_08 |
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