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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927063Generated: November 1, 2026

4-Chlorobenzyl mercaptan → 6-(4-Chlorobenzylthio)-3,4-bis(4-methoxybenzyloxy)pyridazine

https://huagongshe.com/reaction/927063

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzyl mercaptanHCID 80409—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86677026HCID 86677026—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Product6-(4-Chlorobenzylthio)-3,4-bis(4-methoxybenzyloxy)pyridazineHCID 71270229100%

Reaction Steps

A mixture of 6-chloro-3,4-bis[(4-methoxybenzyl)oxy]pyridazine (Intermediate 7; 550 mg, 1.42 mmol), (4-chlorophenyl)methanethiol (248 mg, 1.56 mmol), Pd2(DBA)3 (52.1 mg, 0.057 mmol), XANTPHOS (65.8 mg, 0.114 mmol) and Hunig's base (ethyl diisopropylamine; 404 mg, 3.13 mmol) was subjected to microwave irradiation at 120° C. for 1 hour. The resulting mixture was poured into water and extracted into ethyl acetate before the combined organics were washed with brine and then dried (magnesium sulphate). The resulting solution was evaporated in vacuo and purified by silica chromatography (eluting with 0-40% dichlormethane in petrol) to yield 6-[(4-chlorobenzyl)sulfanyl]-3,4-bis[(4-methoxybenzyl)oxy]pyridazine (201 mg, 1.42 mmol, 28% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290456B2
Source datasetuspto-grants-2016_03
ORD IDord-7adcdf7235f545c788a0c57adc2de7e9
Source noteuspto-grants-2016_03