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HRID 235132作成日:2026年10月25日

Triethylamine → 7-(3-Methylsulfonylaminophenyl)-1-(4-methyl-1-piperazinyl)-naphthalene

https://huagongshe.com/reaction/235132

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Lithium ChlorideHCID 433294—
反応物N-(3-bromophenyl)methanesulfonamideHCID 798932—
反応物7-Trimethylstannyl-1-(4-methyl-1-piperazinyl)-naphthaleneHCID 22115608—
触媒Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物7-(3-Methylsulfonylaminophenyl)-1-(4-methyl-1-piperazinyl)-naphthaleneHCID 2335349435%

反応手順

The title product was prepared following the procedure of example 41 from 7-trimethylstannyl-1-(4-methyl-1-piperazinyl)-naphthalene (0.25 g, 0.67 mmol), 3-methylsulfonylamino-1-bromobenzene (0.18 g, 0.72 mmol), triethylamine (0.45 mL, 3.23 mmol), lithium chloride (0.088 g, 2.07 mmol), and bis (triphenylphosphine) palladium chloride (0.025 g, 0.036 mmol) in DMF (12.5 mL) with a heating time of 1.5 hours. The product was obtained in 35% yield. A sample was obtained by recrystallization from ethyl acetate for analysis: mp 100°-101 ° C. Analysis calculated for C22H25N3O2S·1.5 H2O: C, 62.54; H, 6.68; N, 9.94. Found: C, 62.70; H, 6.46; N, 9.89.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05597826
出典データセットuspto-grants-1997_01
ORD IDord-f1b3340104194543a7b395969cc8330f
出典メモuspto-grants-1997_01