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HRID 227096作成日:2026年10月25日

Triethylamine → 3-(6-Amino-pyridine-3-carbonyl)-1-(6-bromo-pyridin-2-ylmethyl)-1H-quinolin-4-one

https://huagongshe.com/reaction/227096

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Sodium AzideHCID 33557—
反応物Tris(2-carboxyethyl)phosphine hydrochlorideHCID 2734570—
反応物HCID 57754507HCID 57754507—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-(6-Amino-pyridine-3-carbonyl)-1-(6-bromo-pyridin-2-ylmethyl)-1H-quinolin-4-oneHCID 5775457562.7%

反応手順

100 mg (0.22 mmol) of 1-(6-bromo-pyridin-2-ylmethyl)-3-(6-chloro-pyridine-3-carbonyl)-1H-quinolin-4-one and 72 mg (1.1 mmol) of sodium azide were heated at 100° C. in 1 mL of DMF for 1 h. The temperature of the solution was lowered to 70° C. and 1 mL of water was added, followed by 214 uL (155 mg, 1.54 mmol) of triethylamine and 378 mg (1.32 mmol) of tris(2-carboxyethyl)phosphine hydrochloride. After 1 h of reaction time the mixture was purified on reverse-phase HPLC, followed by flash chromatography to give 60 mg of a yellow powder. LC-MSD, m/z for C21H15BrN4O2 [M+H]+=435.0, 437.0; HPLC retention time: 0.6 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557213B2
出典データセットuspto-grants-2009_07
ORD IDord-dc87f762a0db4bc2bd90e8387eb501ca
出典メモuspto-grants-2009_07