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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503543Generated: October 31, 2026

p-Toluenesulfonic acid monohydrate → N-(4-(1,5-naphthyridin-4-ylthio)phenyl)-4-(4-chlorophenyl)phthalazin-1-amine

https://huagongshe.com/reaction/503543

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 4736943HCID 4736943—
Reactant4-(1,5-Naphthyridin-4-ylthio)benzenamineHCID 59427301—
Solventtert-ButanolHCID 6386—
ProductN-(4-(1,5-naphthyridin-4-ylthio)phenyl)-4-(4-chlorophenyl)phthalazin-1-amineHCID 67318825—

Reaction Conditions

Temperature100 °C

Reaction Steps

1-Chloro-4-(4-chlorophenyl)phthalazine (30 mg, 109 μmol), p-toluenesulfonic acid monohydrate (10 mg, 55 μmol) and 4-(1,5-naphthyridin-4-ylthio)benzenamine (33 mg, 131 μmol) were combined in t-butanol in a sealed tube and the reaction mixture was stirred at 100° C. for 2 h. The mixture was concentrated in vacuo and the crude material was purified by silica gel chromatography (0 to 100% 90/10/1 CH2Cl2/MeOH/NH4OH) in CH2Cl2. The material was further purified by silica gel chromatography (0 to 100% EtOAc/hexane) to afford N-(4-(1,5-naphthyridin-4-ylthio)phenyl)-4-(4-chlorophenyl)phthalazin-1-amine. MS [M+H]=492; Calc'd 491.99 for C28H18ClN5S.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776857B2
Source datasetuspto-grants-2010_08
ORD IDord-50fe5bcdf8c946f7b65af863e17c1afd
Source noteuspto-grants-2010_08