HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483155Generated: October 31, 2026
HCID 117857709, compound → HCID 117857548, compound
https://huagongshe.com/reaction/1483155
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 117857709 | HCID 117857709 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 117857548 | HCID 117857548 | 87.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09416137B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-fc31758dead94022b6af873e11834121 |
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| Source note | uspto-grants-2016_08 |
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