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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722456Generated: November 1, 2026

HCID 86742936, compound → HCID 86742937, compound

https://huagongshe.com/reaction/1722456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86742936HCID 86742936—
ReactantHCID 178418361HCID 178418361—
CatalystLindlars catalystHCID 131709914—
SolventMethanolHCID 887—
ProductHCID 86742937HCID 8674293744.7%

Reaction Steps

A mixture of 1-ethyl-8-(1-propynyl)-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid, methyl ester (155 mg, 0.5 mmol), Lindlar catalyst (15 mg), and methanol (10 mL) was charged with 1 atmosphere of hydrogen and allowed to stir at room temperature overnight. The catalyst was then removed by filtration through a celite plug, and the filtrate concentrated to give 170 mg of the crude product. This material was purified by flash chromatography (10% ethyl acetate/hexane, silica gel) to give the pure title compound as yellow oil (70 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855445
Source datasetuspto-grants-1989_08
ORD IDord-62cab3529e214883810d9f6909c10989
Source noteuspto-grants-1989_08