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HRID 10249作成日:2026年10月24日

Allyl Alcohol → 4-i-Propyl-phenyl sulfamic acid-[6-allyloxy-5-(o-methoxyphenoxy)-2-(4-pyridyl)pyrimidin-4-yl]-amide

https://huagongshe.com/ja/reaction/10249

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl AlcoholHCID 7858—
反応物TetrahydrofuranHCID 8028—
反応物Sodium hydrideHCID 24758—
反応物4-i-Propyl-phenyl sulfamic acid-[6-chloro-5-(o-methoxy-phenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-amideHCID 10279868—
溶媒DimethylformamideHCID 6228—
生成物4-i-Propyl-phenyl sulfamic acid-[6-allyloxy-5-(o-methoxyphenoxy)-2-(4-pyridyl)pyrimidin-4-yl]-amideHCID 21979588—

反応条件

温度80 °C

反応手順

To a mixture of allyl alcohol (1 ml) and THF (2 ml) was added sodium hydride (100 mg, 60% dispersion in mineral oil) followed by the addition of 4-i-propyl-phenyl sulfamic acid-[6-chloro-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide (100 mg, Referential Example 1e)). DMF (0.5 ml) was added and the reaction mixture was heated to 80° C. for 20 h. The solvents were evaporated, water (14 ml) and a 10% solution of citric acid was added until the pH was 3. The precipitate was filtered off and washed with water and purified by chromatography through silicagel with EtOAc/Hex=3:2 to give 4-i-propyl-phenyl sulfamic acid-[6-allyloxy-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide (10 mg). tR=5.36 min, (LC); [M+H]+=548.46 (ES+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094781B2
出典データセットuspto-grants-2006_08
ORD IDord-a308b8d7315b46f3a3735372c111dddd
出典メモuspto-grants-2006_08