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HRID 2044880作成日:2026年10月26日

Diisopropylethylamine → N-(1-(5-Chloro-2-(pyridin-2-yl)quinolin-3-yl)ethyl)-9H-purin-6-amine

https://huagongshe.com/reaction/2044880

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Purine, 6-bromo-HCID 5287830—
反応物1-(5-Chloro-2-(pyridin-2-yl)quinolin-3-yl)ethanamineHCID 57707943—
溶媒1-ButanolHCID 263—
生成物N-(1-(5-Chloro-2-(pyridin-2-yl)quinolin-3-yl)ethyl)-9H-purin-6-amineHCID 17846352869%

反応条件

温度110 °C

反応手順

Added 1-(5-chloro-2-(pyridin-2-yl)quinolin-3-yl)ethanamine (103 mg, 363 μmol), 6-bromopurine (72 mg, 363 μmol), n-butanol (2 mL) and DIPEA (190 μl, 1089 mmol) to a 10 mL flask. Submerged in an oil bath and heated at 110° C. for 40 h. The reaction mixture was concentrated on the rotavap to ˜0.5 mL of solvent, diluted with DCM, and chromatographed with 0-15% MeOH:DCM on 12 g silica gel column. The desired fractions were combined and concentrated to an oil which was dissolved in ACN:H2O and lyophilized to obtained 100 mg (69%) of a light tan solid. LC-MS (+esi, M+H+=402.1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08586739B2
出典データセットuspto-grants-2013_11
ORD IDord-f782fadba06e424eb863f6c2c11c11b5
出典メモuspto-grants-2013_11