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HRID 9490作成日:2026年10月24日

Potassium Carbonate → Tert-butyl {4-[(3-amino-7-bromoquinolin-4-ylamino)methyl]benzyl}carbamate

https://huagongshe.com/ja/reaction/9490

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Sodium DithioniteHCID 24489—
反応物Tert-butyl {4-[(7-bromo-3-nitroquinolin-4-ylamino)methyl]benzyl}carbamateHCID 21984421—
触媒1,1'-Diethyl-4,4'-bipyridinium dibromideHCID 11474262—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl {4-[(3-amino-7-bromoquinolin-4-ylamino)methyl]benzyl}carbamateHCID 21984367100.5%

反応手順

Ethyl viologen dibromide (0.069 g, 0.18 mmol), potassium carbonate (12.76 g, 92 mmol) in water (55mL), and sodium hydrosulfite (11.25 g, 65 mmol) in water (55mL) were added sequentially to a solution of tert-butyl{4-[(7-bromo-3-nitroquinolin-4-ylamino)methyl]benzyl}carbamate (9.0 g, 18.5 mmol) in dichloromethane (110 mL). The resulting biphasic mixture was stirred for 20 hours. The reaction was diluted with water (600 mL) and dichloromethane (500 mL). The layers were separated and the aqueous fraction was extracted with dichloromethane. The organic fractions were combined and washed sequentially with water and saturated aqueous sodium chloride. The organic fraction was dried over sodium sulfate, filtered, and concentrated under reduced pressure to yield 8.5 g of tert-butyl{4-[(3-amino-7-bromoquinolin-4-ylamino)methyl]benzyl}carbamate as a yellow-brown amorphous solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091214B2
出典データセットuspto-grants-2006_08
ORD IDord-e14b4f690e7d423e92497dc07775b581
出典メモuspto-grants-2006_08