HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480044Generated: October 30, 2026
HCID 15548678, compound → HCID 15548679, compound
https://huagongshe.com/reaction/480044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 15548678 | HCID 15548678 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 15548679 | HCID 15548679 | 19.9% |
Reaction Steps
To a solution of 2-benzyl-1′-tert-butoxycarbonyl-1′,6′-dihydrospiro[1H-isoindole-1,4′(5′H)-pyridine]-3(2H)-one (1.0 g) in chloroform (20 mL), trifluoroacetic acid (20 mL) was added and the mixture was stirred for 1 hour. The reaction mixture was concentrated. The residue was dissolved in methanol and hydrogenated with 4M hydrogen chloride/ethyl acetate in the presence of 20% palladium carbon at 1 atm of hydrogen for 14 hours. The catalyst was removed by filtration and the filtrate was concentrated. To the residue, aqueous 1N sodium hydroxide (5 mL), di-tert-butyl dicarbonate (655 mg) and dioxane (10 mL) were added and the mixture was stirred at room temperature for 4 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was dried over anhydrous Na2SO4 and concentrated. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=4/1 to 1/2) to give the subject compound (200 mg).
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-7cd216ac72e64389821730d8f2c70356 |
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| Source note | uspto-grants-2003_11 |
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