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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970054Generated: November 3, 2026

Ammonium formate → 8-(3-hydroxy-3-methyl-butyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline 1-ethyl carboxylate

https://huagongshe.com/reaction/1970054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant8-(3-hydroxy-3-methyl-but-1-ynyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline 1-ethyl carboxylateHCID 86627556—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product8-(3-hydroxy-3-methyl-butyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline 1-ethyl carboxylateHCID 8662756010.4%

Reaction Steps

A suspension of 47 mg (0.14 mmol) of 8-(3-hydroxy-3-methyl-but-1-ynyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate, 164 mg (2.6 mmol) of ammonium formate and 5 mg of palladium on charcoal in 10 ml of ethanol is refluxed for 8 hours. The solution is filtered on celite and then evaporated. Water is added and the product is extracted twice with ethyl acetate. The organic phases are dried over magnesium sulfate, filtered and evaporated to give 5 mg (10%) of 8-(3-hydroxy-3-methyl-butyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426437B2
Source datasetuspto-grants-2013_04
ORD IDord-71288c6909644284851c4706873e35b7
Source noteuspto-grants-2013_04