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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 498235Generated: October 30, 2026

Thionyl Chloride → HCID 69486831, compound

https://huagongshe.com/reaction/498235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-Chloro-6-methoxypyridazineHCID 74403—
Reactant3-Carboxyphenylboronic acidHCID 2733957—
ReactantHCID 69489774HCID 69489774—
SolventAcetonitrileHCID 6342—
SolventSodium CarbonateHCID 10340—
ProductHCID 69486831HCID 69486831—

Reaction Steps

The title compound was prepared from 3-(6-methoxy-pyridazin-3-yl)-benzoic acid methyl ester [prepared by the following procedure: A mixture of 3-carboxyphenyl-boronic acid (7.11 g, 42.8 mmol) and 3-chloro-6-methoxy-pyridazine [CAS-No. 1722-10-7] (6.19 g, 42.8 mmol) in acetonitrile (212 mL) and 0.4M Na2CO3-solution (212 mL) was degassed and Pd(Ph3P)4 (2.47 g, 5 mol %) was added. The reaction mixture was refluxed for 16 h, evaporated to dryness (cf. Synlett 2000, 829). The residue was suspended in MeOH (630 mL) and SOCl2 (15.5 mL, 214.1 mmol) was added dropwise at 23° C. and the reaction mixture was refluxed for 4 h. Evaporated to dryness, taken up in EtOAc, washed with sat. NaHCO3-solution and brine, dried over Na2SO4. Removal of the solvent in vacuum left a brown oil, which was purified by silica gel column chromatography with cyclohexane/EtOAc.] (5.41 g, 22.15 mmol) by treatment with lithium tert-butyl acetate according to general procedure K (method b). Obtained as a yellow oil (6.39 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949542B2
Source datasetuspto-grants-2005_09
ORD IDord-518389f48b674ecc9060e13c3755c285
Source noteuspto-grants-2005_09