戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 906282作成日:2026年10月25日

3-(tert-Butylaminosulphonyl)benzeneboronic acid → 3-{4-[4-Difluoromethyl-6-(6-trifluoromethyl-pyridin-3-yl)-pyrimidin-2-yl]-pyridin-2-yl}-benzenesulfonic acid tert-butylamide

https://huagongshe.com/reaction/906282

反応式

関与物質

役割名称HCID仕込み量
反応物3-(tert-Butylaminosulphonyl)benzeneboronic acidHCID 44119538—
反応物2-(2-Chloro-pyridin-4-yl)-4-difluoromethyl-6-(6-trifluoromethyl-pyridin-3-yl)-pyrimidineHCID 86624633—
生成物3-{4-[4-Difluoromethyl-6-(6-trifluoromethyl-pyridin-3-yl)-pyrimidin-2-yl]-pyridin-2-yl}-benzenesulfonic acid tert-butylamideHCID 67393345—

反応手順

3-{4-[4-Difluoromethyl-6-(6-trifluoromethyl-pyridin-3-yl)-pyrimidin-2-yl]-pyridin-2-yl}-benzenesulfonic acid tert-butylamide was prepared from 2-(2-chloro-pyridin-4-yl)-4-difluoromethyl-6-(6-trifluoromethyl-pyridin-3-yl)-pyrimidine (example B.7) (0.19 g, 0.5 mmol) and commercially available 3-(tert.-butylsulfamoyl)-phenylboronic acid (0.15 g, 0.6 mmol) according to the general procedure III. Obtained as off-white solid (0.16 g), which was subsequently deprotected.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08012986B2
出典データセットuspto-grants-2011_09
ORD IDord-c87e5723b3184d71af331021df499c08
出典メモuspto-grants-2011_09