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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107086Generated: October 31, 2026

HCID 86744006, compound → HCID 23047442, compound

https://huagongshe.com/reaction/2107086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86744006HCID 86744006—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 23047442HCID 23047442103.8%

Reaction Steps

A solution of ethyl (E)-5-hydroxy-7-(3-isopropyl-1-phenylpyrrolo[2,1-a]isoquinolin-2-yl)-3-oxohept-6-enoate (0.94 g; prepared as described in Reference Example 2) in ethanol (42 ml) was reduced catalytically under a hydrogen atmosphere using 5% w/w palladium on charcoal (0.254 g) and 5% w/w palladium on calcium carbonate (0.226 g) as catalysts. The mixture was filtered to remove the catalysts and the filtrate was evaporated, to give ethyl 5-hydroxy-7-(3-isopropyl1-phenylpyrrolo[2,1-a]isoquinolin-2-yl)-3-oxoheptanoate (0.98 g) in the form of a pale green gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933350
Source datasetuspto-grants-1990_06
ORD IDord-4cb620aa4dec458381af4cc68aabc339
Source noteuspto-grants-1990_06