Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 178517175 | HCID 178517175 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178514300 | HCID 178514300 | — |
Reaction Steps
To a flask was added 6-chloro-3-phenylpyrido[2,3-b]pyrazin-2-ol (8-2, 3.41 g, 13.23 mmol), anhydrous hydrazine (5.0 mL, 159 mmol), and finally 1.4 Dioxane (60 mL). The stirred reaction mixture was then heated to 100° C. in a hot oil bath under an atmosphere of nitrogen with an air cooled reflux condenser attached. Upon completion of the reaction the mixture was cooled to room temperature, suspended in ethyl acetate and washed with a saturated solution of sodium bicarbonate, followed by water, then brine, dried over sodium sulfate, filtered, and concentrated in vacuo to give 8-3 as an orange/tan foam. HRMS (M+H)+: observed=254.1041, calculated=254.1037.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576209B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-24870a4d9b304e21ac388ce7078d7cd8 |
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| Source note | uspto-grants-2009_08 |
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