HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480060Generated: October 26, 2026
Water → N-[5-(3-hydroxyphenyl)-2-pyrazinyl]-3-oxospiro[isobenzofuran-1(3H),4'-piperidine]-1'-carboxamide
https://huagongshe.com/reaction/480060
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3H-spiro[isobenzofuran-1,4'-piperidin]-3-one hydrochloride | HCID 22380631 | — |
| Reactant | Phenyl N-[5-(3-hydroxyphenyl)-2-pyrazinyl]carbamate | HCID 22660683 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-[5-(3-hydroxyphenyl)-2-pyrazinyl]-3-oxospiro[isobenzofuran-1(3H),4'-piperidine]-1'-carboxamide | HCID 22660746 | 34.7% |
Reaction Steps
A mixture of spiro[isobenzofuran-1(3H),4′-piperidine]-3-one hydrochloride (40 mg), phenyl N-[5-(3-hydroxyphenyl)-2-pyrazinyl]carbamate (51 mg) and triethylamine (119 μL) in chloroform (5 mL) was stirred at 80° C. for 2 hours. The reaction mixture was poured into water and extracted with chloroform (20 mL). The organic layer was washed with saturated saline solution (20 mL) and then dried over anhydrous Na2SO4. The concentration of the solvent left a residue, which was purified by column chromatography on silica gel (hexane/ethyl acetate=4/1 to 1/2) followed by recrystallization from ethyl ether-hexane to give the subject compound (24 mg) as colorless crystals (melting point 257-259° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06649624B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-76cccf61cc7e4ebdba24d0604d42b03c |
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| Source note | uspto-grants-2003_11 |
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