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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797715Generated: November 4, 2026

HCID 22176382, compound → HCID 22176095, compound

https://huagongshe.com/reaction/1797715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22176382HCID 22176382—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22176095HCID 2217609596.5%

Reaction Steps

A suspension of tert-butyl[6-(benzyloxy)-2-isobutyl-1-oxo-4-(2-thienyl)-1,2-dihydro-3-isoquinolinyl]methylcarbamate (1.04 g, 2 mmol) and 5% palladium carbon (1.0 g) in ethanol (10 ml) and tetrahydrofuran (10 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-(2-thienyl)-1,2-dihydro-3-isoquinolinyl]methylcarbamate (0.82 g, 96.5%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034039B2
Source datasetuspto-grants-2006_04
ORD IDord-855ab626a88f460e8e99ad31de243737
Source noteuspto-grants-2006_04