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HRID 39472作成日:2026年10月24日

1,3-Propanediol → 1-(benzo[d][1,3]dioxol-5-yl)-N-(5-((3-hydroxypropoxy)(2-methoxyphenyl)methyl)pyridin-2-yl)cyclopropanecarboxamide

https://huagongshe.com/ja/reaction/39472

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-PropanediolHCID 10442—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物1-(benzo[d][1,3]dioxol-5-yl)-N-(5-(hydroxy(2-methoxyphenyl)methyl)pyridin-2-yl)cyclopropanecarboxamideHCID 44236599—
溶媒TolueneHCID 1140—
生成物1-(benzo[d][1,3]dioxol-5-yl)-N-(5-((3-hydroxypropoxy)(2-methoxyphenyl)methyl)pyridin-2-yl)cyclopropanecarboxamideHCID 4423670455.6%

反応条件

温度140 °C

反応手順

1-(Benzo[d][1,3]dioxol-5-yl)-N-(5-(hydroxy(2-methoxyphenyl)methyl)pyridin-2-yl)cyclopropanecarboxamide (41.8 mg, 0.100 mmol) was suspended in 2 mL of toluene containing 4-methylbenzenesulfonic acid hydrate (pTsOH, 23.8 mg, 0.125 mmol) and propane-1,3-diol (9.89 mg, 0.130 mmol). The reaction mixture was then heated to 140° C. for 5 minutes in a microwave reactor. The crude product was then filtered, evaporated to dryness, dissolved in N,N-dimethylformamide (1 mL) and purified by reverse-phase preparative liquid chromatography utilizing a gradient of 0-99% acetonitrile in water containing 0.05% trifluoroacetic acid to yield the pure product (26.5 mg, 0.0556 mmol, 55.6%). ESI-MS m/z calc. 476.5. found 477.3 (M+1)+. Retention time 2.71 minutes.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524910B2
出典データセットuspto-grants-2013_09
ORD IDord-9bb4882d04c64757999896921400792b
出典メモuspto-grants-2013_09