HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879692Generated: October 30, 2026
Cyclopropylboronic acid → 8-Benzyl-3-cyclopropyl-6,7,8,9-tetrahydropyrazino[2,3-f][1,4]oxazepine
https://huagongshe.com/reaction/1879692
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | Tricyclopropylphosphane | HCID 12716772 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 8-Benzyl-3-chloro-6,7,8,9-tetrahydropyrazino[2,3-f][1,4]oxazepine | HCID 86648981 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 8-Benzyl-3-cyclopropyl-6,7,8,9-tetrahydropyrazino[2,3-f][1,4]oxazepine | HCID 66993315 | 16% |
Reaction Steps
A suspension of 8-benzyl-3-chloro-6,7,8,9-tetrahydropyrazino[2,3-f][1,4]oxazepine (493 mg), cyclopropylboronic acid (280 mg), palladium acetate (20 mg), tricyclopropylphosphine (51 mg) and potassium tert-butoxide (663 mg) in toluene (8 mL) was stirred under an argon atmosphere with heating at 100° C. for 2 hr. Water was added to the reaction mixture, the aqueous layer was extracted with ethyl acetate, and the organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient: 5→25% ethyl acetate/hexane) to give the title compound (79.9 mg, 16%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318722B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-9133956037c54a748f722a7893348809 |
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| Source note | uspto-grants-2012_11 |
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