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HRID 81641作成日:2026年10月26日

(2R)-2-(tetrahydro-2H-pyran-2-yloxy)propyl methanesulfonate → 6-[(5-{[(2R)-2-(methylamino)propyl]oxy}pyridin-2-yl)oxy]-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amine

https://huagongshe.com/reaction/81641

反応式

関与物質

役割名称HCID仕込み量
反応物(2R)-2-(tetrahydro-2H-pyran-2-yloxy)propyl methanesulfonateHCID 59627468—
反応物Methylamine tetrahydrofuranHCID 66615946—
反応物6-({4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-yl}oxy)pyridin-3-olHCID 68429877—
生成物6-[(5-{[(2R)-2-(methylamino)propyl]oxy}pyridin-2-yl)oxy]-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amineHCID 59508836—

反応手順

Using 6-({4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-yl}oxy)pyridin-3-ol obtained in Example 6-3), (2R)-2-(tetrahydro-2H-pyran-2-yloxy)propyl methanesulfonate and 2 M methylamine/tetrahydrofuran solution, and in the same manner as in Example 26 or according to a method similar to it or according to a combination thereof with an ordinary method, the entitled compound (6 mg) was obtained as a pale yellow amorphous solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846700B2
出典データセットuspto-grants-2014_09
ORD IDord-c67919467e9f4da8beae6a58ff060b04
出典メモuspto-grants-2014_09