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HRID 44413作成日:2026年10月25日

Triethylamine → N-(1-Benzyl-4-methylpiperidin-3-yl)-N-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine

https://huagongshe.com/reaction/44413

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1-benzyl-N,4-dimethylpiperidin-3-amineHCID 9943889—
反応物HCID 178418725HCID 178418725—
生成物N-(1-Benzyl-4-methylpiperidin-3-yl)-N-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 1208482950%

反応条件

温度100 °C

反応手順

A solution of 4-chloropyrrolo[2,3-d]pyrimidine (2.4 grams, 15.9 mmol), prepared by the method of Davoll, J. Am. Chem. Soc., 82, 131 (1960), which is incorporated by reference in its entirety, and the product from Method A (1.7 grams, 7.95 mmol) dissolved in 2 equivalents of triethylamine was heated in a sealed tube at 100° C. for 3 days. Following cooling to room temperature and concentration under reduced pressure, the residue was purified by flash chromatography (silica; 3% methanol in dichloromethane) affording 1.3 grams (50%) of the title compound as a colorless oil. LRMS: 336.1 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541426B2
出典データセットuspto-grants-2013_09
ORD IDord-90ce4c8ad50f4e4aa7af55ff18e28333
出典メモuspto-grants-2013_09