戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 448106作成日:2026年10月25日

Pyridine → 4-tert-butyl-N-[4-chloro-2-(5-isopropoxymethyl-[1,3,4]oxadiazol-2-yl)-phenyl]-benzenesulfonamide

https://huagongshe.com/reaction/448106

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Thionyl ChlorideHCID 24386—
反応物4-tert-butyl-N-{4-chloro-2-[N'-(2-isopropoxy-acetyl)-hydrazinocarbonyl]-phenyl}-benzenesulfonamideHCID 66905607—
溶媒Diethyl EtherHCID 3283—
生成物4-tert-butyl-N-[4-chloro-2-(5-isopropoxymethyl-[1,3,4]oxadiazol-2-yl)-phenyl]-benzenesulfonamideHCID 66905277—

反応手順

Thionyl chloride was added to a solution of 4-tert-butyl-N-{4-chloro-2-[N′-(2-isopropoxy-acetyl)-hydrazinocarbonyl]-phenyl}-benzenesulfonamide (150 mg, 0.312 mmol) and pyridine (66 μL, 0.811 mmol) in diethyl ether (3 mL). The resultant solution was stirred for 18 h at room temperature followed by removal of the volatiles in vacuo. 2 mL toluene was subsequently added and the reaction was heated at reflux for 5 h. The resultant solution was concentrated at reduced pressure and the residue purified via flash column chromatography (0-50% ethyl acetate in hexane) to afford 4-tert-butyl-N-[4-chloro-2-(5-isopropoxymethyl-[1,3,4]oxadiazol-2-yl)-phenyl]-benzenesulfonamide as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481579B2
出典データセットuspto-grants-2013_07
ORD IDord-410361b1d2ca4cffae6567c708c06195
出典メモuspto-grants-2013_07