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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110707Generated: October 26, 2026

Sodium Hydroxide → (+/-)-trans-2-Pyrrolidino-6-propyl-5,5a, 6,7,8,9,9a,10-octahydropyrido[2,3-g]quinoline

https://huagongshe.com/reaction/1110707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPyrrolidine, hydrochloride (1:1)HCID 212848—
ReactantHCID 18640062HCID 18640062—
SolventWaterHCID 962—
Product(+/-)-trans-2-Pyrrolidino-6-propyl-5,5a, 6,7,8,9,9a,10-octahydropyrido[2,3-g]quinolineHCID 1864006953.1%

Reaction Conditions

Temperature210 °C

Reaction Steps

A mixture of (±)-trans-2-chloro-6-propyl-5,5a,6,7,8,9,9a,10-octahydropyrido[2,3-g]quinoline hydrochloride (2.50 g, 8.3 mmol) and pyrrolidine hydrochloride (10 g) was heated to 210° C. to form a homogeneous molten semi-solid. After 45 minutes the molten semi-solid was poured into water, made basic with dilute NaOH solution, and extracted with methylene chloride. The extract was dried (Na2SO4) and concentrated to give the crude product as a brown solid. Purification by flash chromatography (10% methanol in methylene chloride, NH4OH) provided (±)-trans-2-pyrrolidino-6-propyl-5,5a,6,7,8,9,9a,10-octahydropyrido[2,3-g]quinoline (Rf =0.45, 1.32 g, 53% yield) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977149
Source datasetuspto-grants-1990_12
ORD IDord-2b861294b5d04ef0b9ffaf58577a3838
Source noteuspto-grants-1990_12