참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Phosphorus oxybromide | HCID 24613 | — |
| 반응물 | 1,4-Dihydroxy-isoquinoline-3-carboxylic acid butyl ester | HCID 178450843 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 1-Bromo-4-hydroxy-isoquinoline-3-carboxylic acid butyl ester | HCID 86014541 | 3.9% |
반응 단계
2 g (7.7 mmol) of 1,4-Dihydroxy-isoquinoline-3-carboxylic acid butyl ester (from Example D-20 b) dissolved in 100 ml of acetonitrile. 15.4 g (53.6 mmol) of phosphorous oxybromide added to solution and mixture stirred at 80° C. for 64 h. 100 ml of water was added to mixture, and mixture was removed from heat. Mixture was partitioned between ethyl acetate and water. Two phases were separated and the aqueous layer was extracted with ethyl acetate. Organic layers were combined, washed with brine, dried over magnesium sulfate, filtered, and evaporated. Residue was purified by silica gel flash chromatography to give 0.1 g (0.3 mmol) of product. 1H NMR (200 MHz, CDCl3) δ 11.89 (s, 1H), 8.41 (m, 1H), 8.25 (m, 1H), 7.84 (m, 2H), 4.49 (t, J=7.0 Hz, 2H), 1.87 (m, 2H), 1.47 (m, 2H), 1.00 (t, J=7.2 Hz, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07863292B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-10cff72e97344bb4b8e20239bd6c170d |
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| 출처 메모 | uspto-grants-2011_01 |
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