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HRID 1473402作成日:2026年10月26日

Benzyl mercaptan → 6-(Benzylthio)-1-(2-methoxy-4-(trifluoromethyl)phenyl)phthalazine

https://huagongshe.com/reaction/1473402

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl mercaptanHCID 7509—
反応物Potassium CarbonateHCID 11430—
反応物DiisopropylethylamineHCID 81531—
反応物1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
反応物6-Bromo-1-chlorophthalazineHCID 22030424—
反応物(2-Methoxy-4-(trifluoromethyl)phenyl)boronic acidHCID 24901776—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
触媒HCID 178418807HCID 178418807—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物6-(Benzylthio)-1-(2-methoxy-4-(trifluoromethyl)phenyl)phthalazineHCID 8668744843.1%

反応条件

温度80 °C

反応手順

A solution of 6-bromo-1-chlorophthalazine (0.500 g, 2.053 mmol), Pd2(dba)3 (0.047 g, 0.051 mmol), Xantphos (0.059 g, 0.103 mmol), and n,n-diisopropylethylamine (1.076 ml, 6.16 mmol) in 6 mL of dioxane was heated to 60° C. and was treated with benzyl mercaptan (0.243 ml, 2.053 mmol) drop wise. After stirring for one hour, LC/MS showed product and bis coupled product. (2-methoxy-4-(trifluoromethyl)phenyl)boronic acid (0.407 g, 1.848 mmol), potassium carbonate (1.135 g, 8.21 mmol), PdCl2(dppf)-CH2Cl2 adduct (0.168 g, 0.205 mmol), and 2 mL of water were added and the reaction mixture was heated to 80° C. overnight. LC/MS showed mostly product, so the reaction mixture was allowed to cool to room temperature. The aqueous layer was removed, and the organics were concentrated. Purification of the crude residue by silica gel column chromatography (0 to 100% EtOAc/heptane) gave 6-(benzylthio)-1-(2-methoxy-4-(trifluoromethyl)phenyl)phthalazine (0.340 g, 0.797 mmol, 38.8% yield). m/z (ESI) 427.2 (M+H)+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09012443B2
出典データセットuspto-grants-2015_04
ORD IDord-d9acc66ef21e415a80b17a51e6ebc392
出典メモuspto-grants-2015_04