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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859063Generated: November 1, 2026

Hydrochloric Acid → (Z)-6,8-dihydro-8-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2-phenyl-7H-pyrrolo[2,3-g]benzoxazol-7-one

https://huagongshe.com/reaction/1859063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPiperidineHCID 8082—
Reactant1H-Pyrrole-2-carboxaldehyde, 3-methoxy-HCID 11286466—
Reactant2-Phenyl-6,8-dihydro-oxazolo[5,4-e]indol-7-oneHCID 21253429—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product(Z)-6,8-dihydro-8-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2-phenyl-7H-pyrrolo[2,3-g]benzoxazol-7-oneHCID 9928673—

Reaction Steps

3-Methoxypyrrole-2-carboxaldehyde (13 mg, 0.105 mmol)(Bellamy, supra) and 2-phenyl-6,8-dihydro-oxazolo[5,4-e]-indol-7-one (17 mg, 0.068 mmol)(Starting Material 4) were suspended in a solution of 10% piperidine (Aldrich) in 2-propanol (1 mL). The mixture was heated at reflux for 2 h. The mixture was cooled, poured into water, and the aqueous mixture was made acidic with concentrated hydrochloric acid. The aqueous layer was extracted with ethyl acetate, and the combined organic extracts were washed with water, brine, and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo and the crude product was purified by reverse phase HPLC using acetonitrile-water as solvent. (Yield 10 mg, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06153634
Source datasetuspto-grants-2000_11
ORD IDord-c397d11d534e48758829aa103b2703fa
Source noteuspto-grants-2000_11