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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 498239생성일: 2026년 10월 24일

Acetonitrile → HCID 69487094, 화합물

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

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Thionyl ChlorideHCID 24386—
반응물3-Carboxyphenylboronic acidHCID 2733957—
반응물3-ChloropyridazineHCID 11274989—
반응물3-Pyridazin-3-yl-benzoic acid methyl esterHCID 69489687—
촉매HCID 178418397HCID 178418397—
용매Sodium CarbonateHCID 10340—
생성물HCID 69487094HCID 69487094—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06949542B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-bd369046b6ac47c498f5c8d2b755e567
출처 메모uspto-grants-2005_09