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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179919Generated: October 31, 2026

N,N-Dimethyl-1,3-propanediamine → HCID 10210345, compound

https://huagongshe.com/reaction/2179919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 76327731HCID 76327731—
SolventDimethylformamideHCID 6228—
ProductHCID 10210345HCID 10210345—

Reaction Conditions

Temperature100 °C

Reaction Steps

0.5 g (0.0036 mol) of potassium carbonate, 1 g (0.00189 mol) of 2,4-bis(4-dimethylamino-2-methylquinolin-6-yl)amino-6-chloro-[1,3,5]triazine prepared according to patent W0001561 and 1 ml (0.0078 mol) of N,N-dimethyl-1,3-propanediamine are successively loaded into a 250 ml round-bottomed flask containing 50 ml of DMF, with stirring, and then the mixture is heated for 15 hours at 100° C. The reaction medium is concentrated and taken up in 100 ml of water. The precipitate formed is filtered, washed with 2×50 ml of 0.1N NaOH and then dried. There are thus obtained 1.2 g of N,N′-bis(4-dimethylamino-2-methylquinolin-6-yl)-N″-(3-dimethylaminopropyl)-[1,3,5]triazine, which is purified by flash chromatography on 30 g of silica (35-70 μm), eluting with a mixture (85/10/5) of dichloromethane, methanol and triethylamine. There is thus obtained, after drying under vacuum at 40° C., 0.45 g (41%) of 2,4-bis(4-dimethylamino-2-methylquinolin-6-yl)amino-6-(3-dimethylaminopropyl)-amino-[1,3,5]triazine, in the form of a yellow powder whose characteristics are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06887873B2
Source datasetuspto-grants-2005_05
ORD IDord-04b44672380b4ed1b04d199a04a8c117
Source noteuspto-grants-2005_05