Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221622생성일: 2026년 10월 25일
1,2-Dichloroethane → 7-bromo-1-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)-2-(chloromethyl)-1H-imidazo[4,5-c]quinoline
https://huagongshe.com/reaction/221622
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Dichloroethane | HCID 11 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Ethyl 2-chloroethanecarboximidate hydrochloride | HCID 12470659 | — |
| 반응물 | 7-bromo-N4-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)quinoline-3,4-diamine | HCID 69105440 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 7-bromo-1-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)-2-(chloromethyl)-1H-imidazo[4,5-c]quinoline | HCID 67157483 | — |
반응 단계
A 1-L, three-necked, Morton flask, equipped with overhead stirrer, was charged with 7-bromo-N4-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)quinoline-3,4-diamine (33.4 g, 81.0 mmol) and 1,2-dichloroethane (400 mL) and the mixture was stirred under N2. Ethyl 2-chloroethanimidoate hydrochloride (29.1 g, 184.0 mmol) was then added in portions and the reaction mixture was heated to 70° C. for 3 days. The reaction mixture was then cooled to ambient temperature and treated with CHCl3 (500 mL) and saturated aqueous NaHCO3 solution (700 mL). The layers were separated and the organic portion was concentrated under reduced pressure to give 38 g of 7-bromo-1-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)-2-(chloromethyl)-1H-imidazo[4,5-c]quinoline as a golden solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08207162B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-981adcc57ad14a6dacdb6502098b97d2 |
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| 출처 메모 | uspto-grants-2012_06 |
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