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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483155Generated: October 31, 2026

HCID 117857709, compound → HCID 117857548, compound

https://huagongshe.com/reaction/1483155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 117857709HCID 117857709—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 117857548HCID 11785754887.2%

Reaction Steps

A mixture of (4R,4aS,7aR,12bS)-3-(cyclobutylmethyl)-N-(2,4-dimethoxybenzyl)-4a-hydroxy-7-oxo-2,3,4,4a,5,6,7,7a-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-9-carboxamide (14.4 g, 27.0 mmol) in trifluoroacetic acid was stirred at ambient temperature for 2 hours. The trifluoroacetic acid was removed under reduced pressure and the residue quenched with 300 mL of ammonium hydroxide (6%). The product was extracted twice into dichloromethane (300 mL), the organic phases combined and dried (MgSO4). Filtration and removal of to the solvent under reduced pressure gave (4R,4aS,7aR,12bS)-3-(cyclobutylmethyl)-4a-hydroxy-7-oxo-2,3,4,4a,5,6,7,7a-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-9-carboxamide (9.0 g, 87% yield); LC/MS (M+H)+=383.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416137B2
Source datasetuspto-grants-2016_08
ORD IDord-fc31758dead94022b6af873e11834121
Source noteuspto-grants-2016_08