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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797590Generated: November 3, 2026

HCID 22175901, compound → HCID 22175724, compound

https://huagongshe.com/reaction/1797590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22175901HCID 22175901—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22175724HCID 2217572495.4%

Reaction Steps

A suspension of tert-butyl[6-benzyloxy-2-isobutyl-1-oxo-4-(4,4,4-trifluorobutoxy)-1,2-dihydro-3-isoquinolinyl]methylcarbamate (3.09 g, 5.5 mmol) and 5% palladium carbon (1.0 g) in tetrahydrofuran (20 mL) and ethanol (20 mL) was stirred under a hydrogen atmosphere at room temperature for 2 h. The catalyst was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give tert-butyl[6-hydroxy-2-isobutyl-1-oxo-4-(4,4,4-trifluorobutoxy)-1,2-dihydro-3-isoquinolinyl]methylcarbamate (2.48 g, 95.4%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034039B2
Source datasetuspto-grants-2006_04
ORD IDord-5f1394255e3946dbbc3622bf20a2a92b
Source noteuspto-grants-2006_04