Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 22477192 | HCID 22477192 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 9795266 | HCID 9795266 | — |
Reaction Steps
A mixture of 6-(4-trifluoromethanesulfonyloxyphenyl)-5H-pyrrolo[2,3-b]pyrazine [20 mg, Reference Example 18(e)], dioxane (3 mL) and pyrrolidine (0.2 mL) was heated at 200° C. in a microwave oven for 1 hour. The reaction mixture was then evaporated and the residue was subjected to chromatography on silica eluting with a mixture of ethyl acetate and heptane (1:1, v/v) to give, after trituration with a mixture of ethyl acetate and methanol, the title compound (11 mg) as a yellow solid. MS: 265.1 (MH+). RT=2.92 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943616B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-92aecc8ec25341489dd08031a27d6c27 |
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| Source note | uspto-grants-2011_05 |
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