Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 606314생성일: 2026년 10월 26일
Boron tribromide → 6-hydroxy-1-(5-isopropyl-1H-indazol-4-yl)-3-methyl-isoquinoline-4-carbaldehyde
https://huagongshe.com/reaction/606314
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Boron tribromide | HCID 25134 | — |
| 반응물 | 1-(5-isopropyl-1H-indazol-4-yl)-6-methoxy-3-methyl-isoquinoline-4-carbaldehyde | HCID 86615934 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 6-hydroxy-1-(5-isopropyl-1H-indazol-4-yl)-3-methyl-isoquinoline-4-carbaldehyde | HCID 136341660 | 34.7% |
반응 단계
BBr3 (8.8 g, 35 mmol) is added slowly to a solution of 1-(5-Isopropyl-1H-indazol-4-yl)-6-methoxy-3-methyl-isoquinoline-4-carbaldehyde (842 mg, 2.3 mmol) in DCM (15 ml) at −78° C. The cold bath is removed and the mixture is warmed to room temperature, and then stirred for a further 1 h. The reaction mixture is poured into ice-water mixture and treated with NH4OH (6 ml). The layers are separated and the aqueous layer is extracted with DCM. The combined organic layers are dried (Na2SO4) and evaporated. The residue is chromatographed on silica gel eluting with EtOAc/MeOH (20:1) to give 490 mg of starting material and 276 mg of 6-hydroxy-1-(5-isopropyl-1H-indazol-4-yl)-3-methyl-isoquinoline-4-carbaldehyde. 1H NMR (CDCl3) 10.9 (s, 1H), 8.87 (s, 1H), 7.62-7.42 (m, 4H), 6.99 (d, 1H), 3.09 (s, 3H), 2.73-2.67 (m, 1H), 1.23 (d, 3H), 1.12 (d, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07915288B2 |
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| 출처 데이터셋 | uspto-grants-2011_03 |
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| ORD ID | ord-87572e2fb1c248c6a992207cef683825 |
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| 출처 메모 | uspto-grants-2011_03 |
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