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HRID 269313作成日:2026年10月25日

5-bromo-N-(2-(dimethylamino)ethyl)thiophene-2-sulfonamide → 5-[5-(4-Chloro-3-methyl-phenyl)-7-difluoromethyl-pyrazolo[1,5-a]pyrimidin-3-ylethynyl]-thiophene-2-sulfonic acid (2-dimethylamino-ethyl)-amide

https://huagongshe.com/reaction/269313

反応式

関与物質

役割名称HCID仕込み量
反応物5-bromo-N-(2-(dimethylamino)ethyl)thiophene-2-sulfonamideHCID 8716799—
反応物5-(4-Chloro-3-methyl-phenyl)-7-difluoromethyl-3-ethynyl-pyrazolo[1,5-a]pyrimidineHCID 86608084—
生成物5-[5-(4-Chloro-3-methyl-phenyl)-7-difluoromethyl-pyrazolo[1,5-a]pyrimidin-3-ylethynyl]-thiophene-2-sulfonic acid (2-dimethylamino-ethyl)-amideHCID 67000752—

反応手順

The title compound was prepared from 5-(4-chloro-3-methyl-phenyl)-7-difluoromethyl-3-ethynyl-pyrazolo[1,5-a]pyrimidine (example C.16) (159 mg, 0.5 mmol) and 5-bomo-thiophene-2-sulfonic acid (2-dimethylamino-ethyl)-amide (example B.49) (157 mg, 0.5 mmol) according to general procedure II. Obtained as a yellow solid (200 mg, 73%). MS (ISN) 548.1 [(M−H)−]; mp 149° 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-4265026831da46bf916ad54fc09dd5fb
出典メモuspto-grants-2008_11