Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1-Phenethylpiperazine | HCID 79214 | — |
| Reactant | HCID 22624307 | HCID 22624307 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70105058 | HCID 70105058 | 62% |
Reaction Steps
To a 25 mL round-bottomed flask equipped with condenser and N2 inlet were added 300 mg (0.847 mmol) N-t-butylcarbonyl-6-(2-isopropoxy-4-oxiranylphenyl)-pyridin-2-ylamine, 193 mg (1.017 mmol) N-phenethylpiperazine, 9 mL acetonitrile, and 0.85 mL water. The reaction was heated to 80° C. for 20 hours, cooled, and partitioned between ethyl acetate and aqueous sodium bicarbonate. The organic phase was separated, washed with brine, dried over sodium sulfate, and evaporated. The residue was chromatographed on silica gel using methanol/methylene chloride/ammonium hydroxide as eluant to afford 283 mg (62%) of an off-white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06362195B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-83c775c3b9284919a305c3ca9d31fcd9 |
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| Source note | uspto-grants-2002_03 |
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