戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 498239作成日:2026年10月24日

Acetonitrile → HCID 69487094、化合物

https://huagongshe.com/ja/reaction/498239

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物Thionyl ChlorideHCID 24386—
反応物3-Carboxyphenylboronic acidHCID 2733957—
反応物3-ChloropyridazineHCID 11274989—
反応物3-Pyridazin-3-yl-benzoic acid methyl esterHCID 69489687—
触媒HCID 178418397HCID 178418397—
溶媒Sodium CarbonateHCID 10340—
生成物HCID 69487094HCID 69487094—

反応手順

The title compound was prepared from 3-pyridazin-3-yl-benzoic acid methyl ester [prepared by the following procedure: A mixture of 3-carboxyphenylboronic acid (6.98 g, 42.06 mmol) and 3-chloropyridazine [CAS-No. 1120-95-2] (4.817 g, 42.06 mmol) in acetonitrile (210 ml) and 0.4M Na2CO3-solution (210 ml) was degassed and Pd(Ph3P)4 (2.43 g, 2.1 mmol) was added. The reaction mixture was refluxed for 15 h and evaporated to dryness [Synlett 2000 (6), 829-831]. The residue was suspended in MeOH (500 ml), SOCl2 (15.3 ml, 211 mmol) was added dropwise at 23° C. and the reaction mixture was stirred at reflux for 16 h. Concentrated in vacuum to about 100 mL, diluted with EtOAc, washed with sat. NaHCO3-solution and brine, dried over Na2SO4. Removal of the solvent in vacuum left a brown residue, which was purified by silica gel column chromatography with cyclohexane/EtOAc.] (7.35 g, 34.32 mmol) by treatment with lithium tert-butyl acetate according to general procedure K (method b). Obtained as a yellow oil (8.306 g, 81%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06949542B2
出典データセットuspto-grants-2005_09
ORD IDord-bd369046b6ac47c498f5c8d2b755e567
出典メモuspto-grants-2005_09