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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 4-Chloroisoquinolin-5-amine | HCID 21979937 | — |
| 반응물 | Tert-butyl 4-oxo-1-aminocyclohexylcarboxylate | HCID 21979990 | — |
| 촉매 | Titanium isopropoxide | HCID 11026 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(tert-butoxycarbonyl)-N'-(4-chloro-5-isoquinolyl)-1,4-cyclohexanediamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07094789B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-2183330ad69d4daf8b0bf3debc9cee84 |
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| 출처 메모 | uspto-grants-2006_08 |
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