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HRID 592520作成日:2026年10月25日

Water → 5-Bromo-1-methyl-3-(5-(4-(oxetan-3-yl)piperazin-1-yl)pyridin-2-ylamino)pyridin-2(1H)-one

https://huagongshe.com/reaction/592520

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物3-OxetanoneHCID 15024254—
反応物5-Bromo-1-methyl-3-((5-(piperazin-1-yl)-pyridin-2-yl)amino)pyridin-2(1H)-oneHCID 58043665—
触媒ZincchlorideHCID 3007855—
溶媒MethanolHCID 887—
生成物5-Bromo-1-methyl-3-(5-(4-(oxetan-3-yl)piperazin-1-yl)pyridin-2-ylamino)pyridin-2(1H)-oneHCID 5804379461%

反応条件

温度50 °C

反応手順

A mixture of 101j (2.75 g, 7.5 mmol), oxetan-3-one (1.6 g, 22.7 mmol), NaBH3CN (4.75 g, 22.5 mmol), and zinc chloride (3 g, 22.7 mmol) in methanol (125 mL) was stirred for 5 hours at 50° C. The mixture was added to water and extracted with methylene chloride for three times. The organic layers were concentrated under reduced pressure. The residue was purified by column chromatography eluting with 25:1 methylene chloride/methanol to give 101k (1.92 g, 61%). MS: [M+H]+ 420. 1H NMR (500 MHz, DMSO) δ 8.58 (d, J=2.5, 1H), 8.55 (s, 1H), 7.94 (d, J=3, 1H), 7.54 (d, J=2.5, 1H), 7.39 (dd, J=3, 1H), 7.25 (d, J=4, 1H), 4.56 (t, J=6.5, 2H), 4.46 (t, J=6.5, 2H), 3.50 (s, 3H), 3.43 (m, 1H), 3.01 (m, 4H), 2.40 (m, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09238655B2
出典データセットuspto-grants-2016_01
ORD IDord-60c59baeb9324e3583500ad8959936c9
出典メモuspto-grants-2016_01