Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1042269생성일: 2026년 10월 26일
Phosphorus oxychloride → N-(3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyridin-2-yl)-1-chloro-6-methylisoquinolin-5-amine
https://huagongshe.com/reaction/1042269
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Phosphorus oxychloride | HCID 24813 | — |
| 반응물 | 5-(3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1(2H)-one | HCID 59627371 | — |
| 생성물 | N-(3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyridin-2-yl)-1-chloro-6-methylisoquinolin-5-amine | HCID 59627376 | 67.3% |
반응 단계
5-(3-(7H-Pyrrolo[2,3-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1(2H)-one (750 mg, 2036 μmol) was suspended in phosphorous oxychloride (9.5 mL, 10.2 mmol). The reaction vessel was flushed with N2 and sealed. The reaction was heated in an oil bath for 5 h. The excess reagent was removed in vacuo. The residue was azeotroped with toluene times and then put under high vacuum overnight. The residue was suspended with 50 g of ice. The suspension was neutralized with NaHCO3 (aq., sat.). The resulting mixture was extracted with DCM. The DCM solution was concentrated in vacuo and the residue was purified via flash column on silica (Hexane:EtOAc gradient of 50-10%) to give N-(3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyridin-2-yl)-1-chloro-6-methylisoquinolin-5-amine as a yellow solid (530 mg, 67% yield). MS (ESI, pos. ion) m/z: 387 [M+H]+
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08557830B2 |
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| 출처 데이터셋 | uspto-grants-2013_10 |
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| ORD ID | ord-e3100cf83e314e539dea424865e7c4ac |
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| 출처 메모 | uspto-grants-2013_10 |
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