Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503544Generated: October 31, 2026

4-(7-Methoxy-1,5-naphthyridin-4-yloxy)benzenamine → 4-(4,5-dimethylthiophen-2-yl)-N-(4-(7-methoxy-1,5-naphthyridin-4-yloxy)phenyl)phthalazin-1-amine

https://huagongshe.com/reaction/503544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(7-Methoxy-1,5-naphthyridin-4-yloxy)benzenamineHCID 44185106—
Reactant1-Chloro-4-(4,5-dimethylthiophen-2-yl)phthalazineHCID 86628666—
Solventtert-ButanolHCID 6386—
Product4-(4,5-dimethylthiophen-2-yl)-N-(4-(7-methoxy-1,5-naphthyridin-4-yloxy)phenyl)phthalazin-1-amineHCID 67318194—

Reaction Conditions

Temperature100 °C

Reaction Steps

In a nitrogen purged sealed tube, 1-chloro-4-(4,5-dimethylthiophen-2-yl)phthalazine (0.040 g, 0.146 mmol) was dissolved in tert-butanol (1.00 mL). 4-(7-Methoxy-1,5-naphthyridin-4-yloxy)benzenamine (0.039 g, 0.146 mmol) was added, and the reaction mixture in the tube was stirred at 100° C. for 3 h. The mixture was concentrated in vacuo, and the crude material was purified by silica gel chromatography using 0-100% CH2Cl2:MeOH(90:10)/CH2Cl2. Product-containing fractions were concentrated to yield 4-(4,5-dimethylthiophen-2-yl)-N-(4-(7-methoxy-1,5-naphthyridin-4-yloxy)phenyl)phthalazin-1-amine as light yellow solid. MS [N+H]=506.0; Calc'd 505.6 for C29H23N5O2S.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776857B2
Source datasetuspto-grants-2010_08
ORD IDord-1b7a385518344524b3068641746bb65f
Source noteuspto-grants-2010_08