Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 3-(4-tert-Butoxycarbonyl-1-piperazinyl)-2(1H)-pyrazinone | HCID 59013892 | — |
| Reactant | HCID 86591624 | HCID 86591624 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86591623 | HCID 86591623 | — |
Reaction Steps
A mixture of 3-(4-tert-butoxycarbonyl-1-piperazinyl)-2(1H)-pyrazinone (0.83 g, 3.0 mmol; from Example 48, Step 1) and t-BuOK (497 mg, 4.4 mmol) in THF (5 mL) was stirred for 10 min, and then added to methanesulfonic acid 3-(2,4,5-trifluoro-phenoxy)-propyl ester (0.80 g, 3.0 mmol; from Step 2) in THF (50 mL). After being stirred at room temperature for 1 day, HPLC showed about 20% conversion. After 6 days, the reaction was worked up: water was added, THF was evaporated and the aqueous mixture was extracted twice with EtOAc, dried and concentrated to yield 1.33 g of the crude product as a yellow oil. HPLC analysis showed a 1/1 ratio between the title product and the isomeric O-alkylated product. Purification by chromatography on silica gel using EtOAc/hexane (1/3 to 1/1.7) as eluent gave 427 mg (30%) of the title product as a colorless oil. HPLC purity: 96%. MS m/z 469 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244722B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-aff406b0967f4e9b8b2b6616e8c5eb7d |
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| Source note | uspto-grants-2007_07 |
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