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HRID 38080作成日:2026年10月26日

p-Toluenesulfonyl isocyanate → 1-(4-methyl-benzenesulfonyl)-3-[3-(3-pyridin-4-yl-6,7-dihydro-5H-pyrazolo-[5,1-b][1,3]thiazin-2-yl)-phenyl]-urea

https://huagongshe.com/reaction/38080

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonyl isocyanateHCID 77703—
反応物3-(3-Pyridin-4-yl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]thiazin-2-yl)-phenylamineHCID 67422864—
溶媒DichloromethaneHCID 6344—
生成物1-(4-methyl-benzenesulfonyl)-3-[3-(3-pyridin-4-yl-6,7-dihydro-5H-pyrazolo-[5,1-b][1,3]thiazin-2-yl)-phenyl]-ureaHCID 58477105—

反応手順

To a solution of 3-(3-pyridin-4-yl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]thiazin-2-yl)-phenylamine (prepared as described in Example 3) (50 mg, 0.162 mmol) in dichloromethane (5 mL), 4-methyl-benzenesulfonyl isocyanate (28 mg, 0.178 mmol) was added in one portion. The reaction mixture was stirred at room temperature for 2 hours and evaporated to dryness. The reaction mixture was purified by flash chromatography over silica gel using dichloromethane-methanol (97:3) as the eluant system. 1-(4-methyl-benzenesulfonyl)-3-[3-(3-pyridin-4-yl-6,7-dihydro-5H-pyrazolo-[5,1-b][1,3]thiazin-2-yl)-phenyl]-urea was obtained as a colorless solid (21 mg, 32%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524707B2
出典データセットuspto-grants-2013_09
ORD IDord-c492f94afd604fac8010e313b1faff65
出典メモuspto-grants-2013_09