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HRID 10551생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/10551

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물Sodium borohydrideHCID 4311764—
반응물4-Chloroisoquinolin-5-amineHCID 21979937—
촉매Titanium isopropoxideHCID 11026—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물4-(4-Chloro-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 2197985021.8%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094789B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-72438e154c334ea6b03363a7903a683d
출처 메모uspto-grants-2006_08