戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 10551作成日:2026年10月26日

Sodium Bicarbonate → 4-(4-Chloro-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine

https://huagongshe.com/reaction/10551

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
反応物Sodium borohydrideHCID 4311764—
反応物4-Chloroisoquinolin-5-amineHCID 21979937—
触媒Titanium isopropoxideHCID 11026—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物4-(4-Chloro-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 2197985021.8%

反応手順

According to the method of Example 103, Step A, a mixture of Intermediate 90 (121 mg), tert-butyl 4-oxo-1-piperidinecarboxylate (274 mg), titanium tetraisopropoxide (0.41 ml) and dichloromethane (7 ml) was stirred at room temperature for 138 hours. The reaction mixture was added with sodium borohydride (114 mg) and methanol (1 ml) and stirred for 1.5 hours with ice cooling. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate (10 ml) with ice cooling and extracted twice with ethyl acetate (15 ml for each time). The organic layer was dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1) to obtain the title compound (53.5 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094789B2
出典データセットuspto-grants-2006_08
ORD IDord-72438e154c334ea6b03363a7903a683d
出典メモuspto-grants-2006_08