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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070535Generated: October 26, 2026

1-Chloro-4-(4-chlorophenylamino)-phthalazine → 1-(4-Chlorophenylamino)-4-(4-pyridylthio)phthalazine

https://huagongshe.com/reaction/1070535

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(4-chlorophenylamino)-phthalazineHCID 12075649—
Reactantpyridine-4-thiolHCID 178418431—
SolventEthyl AcetateHCID 8857—
Product1-(4-Chlorophenylamino)-4-(4-pyridylthio)phthalazineHCID 22397271—

Reaction Steps

1-Chloro-4-(4-chlorophenylamino)-phthalazine (R. D. Haworth and S. Robinson, J. Chem. Soc. 1948, pp.777-782) (2.00 g; ˜6.12 mmol) can be melted together with one equivalent of 4-mercaptopyridine at about 140° C. for about 10-30 min. to yield a residue which is dissolved in ethyl acetate, washed with aqueous sodium carbonate and then evaporated in vacuo. The residue can be purified by chromatography on silica gel using a gradient of pure methylene chloride to 50% acetone in methylene chloride to yield pure 1-(4-chlorophenylamino)-4-(4-pyridylthio)phthalazine. The intermediate thioether can be stirred as a solution in acetic acid as 30% aqueous hydrogen peroxide is added in small portions until TLC analysis indicates that all starting material has been consumed. The crude product is isolated by dilution with ethyl acetate, washing with aqueous carbonate solution to remove acetic acid and evaporation in vacuo. Pure invention compound can be obtained by chromatography on the residue on silica gel using methylene chloride/acetone gradients.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903101B1
Source datasetuspto-grants-2005_06
ORD IDord-a4921a71952b4d43ad5ea66ca7ff579f
Source noteuspto-grants-2005_06