Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | HCID 88932538 | HCID 88932538 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68313005 | HCID 68313005 | — |
Reaction Steps
A mixture of 1-(1-{4-[1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca1(14),2,4,10,12-pentaen-13-yl}ethyl)azetidin-3-yl methanesulfonate from Example 162 (70 mg, 0.15 mmol) and dimethylamine (68 mg, 1.5 mmol) in 1,4-dioxane (4 mL) was stirred at 80° C. for 16 h under nitrogen atmosphere. After concentration, the residue was purified by reverse phase Combiflash eluting with a 0-50% gradient of CH3CN in 0.3% NH4HCO3 to give 168. The enantiomers were separated by chiral HPLC (OJ-H column, 2% EtOH (0.1% DEA) in n-hexane isocratic) to give: 9 mg of one enantiomer and 5 mg of the other (23% total yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090628B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-e2f4ce726e31454383da1ff32ae633ec |
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| Source note | uspto-grants-2015_07 |
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