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HRID 1750275作成日:2026年10月27日

Dimethylamine → 3-[4-(dimethylamino)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]benzonitrile

https://huagongshe.com/reaction/1750275

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物TriethylamineHCID 8471—
反応物3-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-5-yl)benzonitrileHCID 86706953—
溶媒1-ButanolHCID 263—
生成物3-[4-(dimethylamino)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]benzonitrileHCID 72706841—

反応条件

温度150 °C

反応手順

A mixture of 3-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-5-yl)benzonitrile (C14) (157 mg, 0.616 mmol), dimethylamine (189 mg, 4.19 mmol) and triethylamine (182 mg, 1.80 mmol) in n-butanol (12 mL) was heated under microwave irradiation at 150° C. for 25 minutes. After concentration in vacuo, the residue was purified by preparative HPLC (Column: Phenomenex Gemini C18, 8 μm; Mobile phase A: ammonia in water, pH 10; Mobile phase B: acetonitrile; Gradient: 25% to 65% B) to give the product as a white solid. Yield: 72.1 mg, 0.274 mmol, 44%. LCMS m/z 263.8 [M+H+]. 1H NMR (400 MHz, DMSO-d6) δ 12.15 (br s, 1H), 8.28 (s, 1H), 7.93 (br s, 1H), 7.78 (br d, J=7.8 Hz, 1H), 7.73 (br d, J=7.8 Hz, 1H), 7.62 (br dd, J=8.0, 7.8 Hz, 1H), 7.57 (br s, 1H), 2.73 (s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09156845B2
出典データセットuspto-grants-2015_10
ORD IDord-e0b0d6d48e64499cbabbbb5c55473eb4
出典メモuspto-grants-2015_10