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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503550Generated: October 30, 2026

N1-(4-phenylphthalazin-1-yl)benzene-1,4-diamine → N1-(7-methoxy-1,5-naphthyridin-4-yl)-N4-(4-phenylphthalazin-1-yl)benzene-1,4-diamine

https://huagongshe.com/reaction/503550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN1-(4-phenylphthalazin-1-yl)benzene-1,4-diamineHCID 57756220—
Reactant8-Chloro-3-methoxy-1,5-naphthyridineHCID 59427340—
SolventDimethylformamideHCID 6228—
ProductN1-(7-methoxy-1,5-naphthyridin-4-yl)-N4-(4-phenylphthalazin-1-yl)benzene-1,4-diamineHCID 59427298—

Reaction Conditions

Temperature70 °C

Reaction Steps

In a 20 mL sealed tube was dissolved 8-chloro-3-methoxy-1,5-naphthyridine (70 mg, 360 μmol) in DMF (2.00 mL). To this was added N1-(4-phenylphthalazin-1-yl)benzene-1,4-diamine (124 mg, 396 μmol) and the reaction mixture was stirred at 70° C. for 17 h. Upon cooling to RT, the mixture was dissolved in DMF and purified using Gilson reverse phase chromatography. The product fractions were combined, concentrated and the resulting crude was extracted into DCM, washed 1× sodium carbonate, 1×H2O, dried with Na2SO4, filtered through fritted funnel, concentrated to yield N1-(7-methoxy-1,5-naphthyridin-4-yl)-N4-(4-phenylphthalazin-1-yl)benzene-1,4-diamine as light yellow solid. MS [M+H]=471.0; Calc'd 470.5 for C29H22N6O.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776857B2
Source datasetuspto-grants-2010_08
ORD IDord-c8dccaaa8edc4e258b6ba0cff91fef4a
Source noteuspto-grants-2010_08