戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 407051作成日:2026年10月27日

5-Methyl-1,2-oxazole-4-sulfonyl chloride → N-{3-[7-(1-{3-(Cyanomethyl)-1-[(5-methylisoxazol-4-yl)sulfonyl]azetidin-3-yl}-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-3-yl]phenyl}-N'-(2,2,2-trifluoroethyl)urea

https://huagongshe.com/reaction/407051

反応式

関与物質

役割名称HCID仕込み量
反応物5-Methyl-1,2-oxazole-4-sulfonyl chlorideHCID 2776141—
反応物N-[3-(7-{1-[3-(cyanomethyl)azetidin-3-yl]-1H-pyrazol-4-yl]imidazo[1,2-b]pyridazin-3-yl)phenyl]-N'-(2,2,2-trifluoroethyl)ureaHCID 67980375—
生成物N-{3-[7-(1-{3-(Cyanomethyl)-1-[(5-methylisoxazol-4-yl)sulfonyl]azetidin-3-yl}-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-3-yl]phenyl}-N'-(2,2,2-trifluoroethyl)ureaHCID 57385638—

反応手順

This compound was prepared by using procedures analogous to those described for the synthesis of Example 73, Step 4 starting from N-[3-(7-{1-[3-(cyanomethyl)azetidin-3-yl]-1H-pyrazol-4-yl}imidazo[1,2-b]pyridazin-3-yl)phenyl]-N′-(2,2,2-trifluoroethyl)urea and 5-methylisoxazole-4-sulfonyl chloride. LCMS (M+H)+: m/z=641.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754114B2
出典データセットuspto-grants-2014_06
ORD IDord-a99a88ef4f21485a870712dc1199910e
出典メモuspto-grants-2014_06