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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821090Generated: October 31, 2026

Sodium Bicarbonate → 6-[3-(6-Chloro-1,2,3,4-tetrahydro-acridin-9-ylamino)-propylamino]-5,6,7,8-tetrahydro-1H-quinolin-2-one

https://huagongshe.com/reaction/1821090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(3-aminopropyl)-6-chloro-1,2,3,4-tetrahydroacridin-9-amineHCID 23645224—
Reactant7,8-Dihydroquinoline-2,6(1H,5H)-dioneHCID 54309798—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product6-[3-(6-Chloro-1,2,3,4-tetrahydro-acridin-9-ylamino)-propylamino]-5,6,7,8-tetrahydro-1H-quinolin-2-oneHCID 2498983137%

Reaction Steps

To a mixture of N1-(6-Chloro-1,2,3,4-tetrahydro-acridin-9-yl)-propane-1,3-diamine (50 mg, 0.17 mmoL), 1,5,7,8-Tetrahydro-quinoline-2,6-dione (31 mg, 0.19 mmoL) in 5 mL methylene chloride, was added sodium triacetoxyborohydride (110 mg, 0.52 mmoL) and a catalytic amount of acetic acid. After stiring at room temperature for 24 h, the reaction was stopped by adding saturated sodium bicarbonate. The mixture was extracted with methylene chloride three times. The combined methylene chloride extract was dried, filtered and concentrated. Purification by column chromatography on silica gel column with 10% MeOH/1% ammonium hydroxide in methylene chloride provided the desired product (27.6 mg, 0.063 mmoL, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605265B2
Source datasetuspto-grants-2009_10
ORD IDord-a2fe845b1ddc48e388aec9506ad57c7a
Source noteuspto-grants-2009_10