HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 498235Generated: October 30, 2026
Thionyl Chloride → HCID 69486831, compound
https://huagongshe.com/reaction/498235
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Chloro-6-methoxypyridazine | HCID 74403 | — |
| Reactant | 3-Carboxyphenylboronic acid | HCID 2733957 | — |
| Reactant | HCID 69489774 | HCID 69489774 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | HCID 69486831 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06949542B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-518389f48b674ecc9060e13c3755c285 |
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| Source note | uspto-grants-2005_09 |
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