戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 269200作成日:2026年10月25日

3-bromo-N-methylbenzene-1-sulfonamide → N-Methyl-3-[7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidin-3-ylethynyl]-benzenesulfonamide

https://huagongshe.com/reaction/269200

反応式

関与物質

役割名称HCID仕込み量
反応物3-bromo-N-methylbenzene-1-sulfonamideHCID 7213265—
反応物3-Ethynyl-7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidineHCID 71539732—
生成物N-Methyl-3-[7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidin-3-ylethynyl]-benzenesulfonamideHCID 86608071—

反応手順

The title compound was prepared from 3-ethynyl-7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine (example C.1) (355 mg, 1.0 mmol) and 3-bromo-N-methyl-benzenesulfonamide (example B.32) (225 mg, 1.0 mmol) according to general procedure II. Obtained as a yellow solid (360 mg, 68%). MS (ISP) 525.2 [(M+H)+]; mp 213-214° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07446113B2
出典データセットuspto-grants-2008_11
ORD IDord-d87a71d4d221409499c8e05734effe8e
出典メモuspto-grants-2008_11