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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249817Generated: November 3, 2026

HCID 15548678, compound → HCID 15548679, compound

https://huagongshe.com/reaction/1249817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15548678HCID 15548678—
SolventChloroformHCID 6212—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 15548679HCID 1554867919.9%

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 for4hours. 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06335345B1
Source datasetuspto-grants-2002_01
ORD IDord-275f8db2e562422e91f53f9b9fc867bf
Source noteuspto-grants-2002_01