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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10553생성일: 2026년 10월 26일

Sodium Bicarbonate → N-(tert-butoxycarbonyl)-N'-(4-chloro-5-isoquinolyl)-1,4-cyclohexanediamine

https://huagongshe.com/reaction/10553

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물Sodium borohydrideHCID 4311764—
반응물4-Chloroisoquinolin-5-amineHCID 21979937—
반응물Tert-butyl 4-oxo-1-aminocyclohexylcarboxylateHCID 21979990—
촉매Titanium isopropoxideHCID 11026—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물N-(tert-butoxycarbonyl)-N'-(4-chloro-5-isoquinolyl)-1,4-cyclohexanediamineHCID 21979991—

반응 단계

According to the method of Example 103, Step A, a mixture of Intermediate 90 (100 mg), tert-butyl 4-oxo-1-aminocyclohexylcarboxylate (270 mg), titanium tetraisopropoxide (0.34 ml) and dichloromethane (7 ml) was stirred at room temperature for 120 hours. The reaction mixture was added with sodium borohydride (94 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 then 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 (40.4 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094789B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-2183330ad69d4daf8b0bf3debc9cee84
출처 메모uspto-grants-2006_08