Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Amino-6-Chloropyrazine | HCID 118458 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21075393 | HCID 21075393 | 57.1% |
Reaction Steps
A mixture of allyl alcohol (0.21 mL, 3.08 mmol) in dioxane (4 mL) was treated with NaH (60%, 3.08 mmol), stirred for 30 minutes, treated with 2-amino-6-chloropyrazine (200 mg, 1.54 mmol), heated to 140° C. in a Smith Synthesizer for 2200 seconds, and filtered. The filtrate was concentrated and purified by flash column chromatography eluting with hexanes/ethyl acetate (2:1) to provide the desired product (133 mg, 57%). MS (DCI/NH3) m/z 152.0 (M+H)+; 1H NMR (500 MHz, CD2Cl2) δ 4.75 (m, 2H), 5.24 (m, 1H), 5.37 (m, 1H), 6.05 (m, 1H), 7.50 (s, 1H), 7.53 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163939B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-a924115265384afabb2aa21dd769372c |
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| Source note | uspto-grants-2007_01 |
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