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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975767Generated: October 26, 2026

Ammonium formate → 3-(N-Propionyl)amino-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/1975767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant8-chloro-2-(N-n-propylamino)tetralinHCID 14969229—
ReactantN-(Quinolin-3-Yl)propanamideHCID 19032664—
Reactant7-amino-8-chloro-2-(N-n-propyl-N-propionylamino)tetralinHCID 19377755—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-(N-Propionyl)amino-1,2,3,4-tetrahydroquinolineHCID 19697664—

Reaction Steps

To a solution of 17.4 g (86.9) 3-(N-propionyl)aminoquinoline and 20.0 g (317 mmol) ammonium formate in 150 ml methanol was added 1.0 g Pd/C cautiously under an inert atmosphere. After stirring at ambient temperature for 2 days the reaction stopped. The ratio between starting material and product was approximately 1:1 (monitored by GLC). The mixture was filtered on Celite and evaporated to a residue from which the product was extracted into diethyl ether. The ether solution was dried (magnesium sulfate), filtered and evaporated. The product/starting material mixture was then recharged in a similar manner using the same amounts of reactants. After additional 4 days the reaction was completed and worked-up as above to yield 9.7 g (55%) of reasonably pure material.: MS m/e 204 (M+, 4), 130 (100), 131 (45), 118 (8), 91 (5), 77 (5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05288748
Source datasetuspto-grants-1994_02
ORD IDord-a5d0abc32e6d42d9a8ebd08f72fa7358
Source noteuspto-grants-1994_02