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HRID 215915作成日:2026年10月25日

Diethyl (3-aminopropyl)phosphonate → Diethyl 3-(4-(1-(2-(Dimethylamino)-6-methoxybenzyl)piperidin-4-ylamino)quinazolin-2-ylamino)propylphosphonate

https://huagongshe.com/reaction/215915

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl (3-aminopropyl)phosphonateHCID 78113—
反応物2-Chloro-N-(1-(2-(dimethylamino)-6-methoxybenzyl)piperidin-4-yl)quinazolin-4-amineHCID 58006255—
溶媒1-ButanolHCID 263—
生成物Diethyl 3-(4-(1-(2-(Dimethylamino)-6-methoxybenzyl)piperidin-4-ylamino)quinazolin-2-ylamino)propylphosphonateHCID 58006204—

反応条件

温度117 °C

反応手順

Following General Procedure D, Compound 47 (50 mg, 0.12 mmol) and diethyl 3-aminopropylphosphonate (69 mg, 0.36 mmol) in n-BuOH (3 mL) were heated to 117° C. for 24 h with a reflux condenser. The product (Compound 81) was purified by preparative silica gel TLC plate 1000μ using 5% (7N NH3-MeOH) and 95% CH2Cl2 solution as eluent.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193203B2
出典データセットuspto-grants-2012_06
ORD IDord-ce4843057c1b49bcb9d1098f304d04c1
出典メモuspto-grants-2012_06