참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrogen Bromide | HCID 260 | — |
| 반응물 | Nitrate | HCID 943 | — |
| 반응물 | Urea | HCID 1176 | — |
| 반응물 | Sodium Nitrate | HCID 24268 | — |
| 반응물 | 5-Amino-1-chloroisoquinoline | HCID 459771 | — |
| 촉매 | copper(I) bromide | HCID 24593 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5-Bromo-1-chloroisoquinoline | HCID 21192497 | — |
반응 단계
To a 500 mL round-bottomed flask containing 1-chloroisoquinolin-5-amine (Step 2, 5.8 g, 32.5 mmol) in H2O (33 mL) and 40% HBr (14 mL) chilled to −50 C in an ice bath, was added a freshly prepared solution of (Sodium nitrate (2.47 g, 35.7 mmol) in 8 mL of H2O) drop-wise over 15 minutes. After the addition, the mixture was kept at 2° C., while stirred an additional 20 minutes. Then urea (0.192 g, 3.2 mmol) was added in order to decompose excess nitrate in the reaction mixture. After an additional 5 minutes of stirring the diazonium salt mixture was transferred into a dropping funnel. The diazonium salt was added drop-wise into a heated (70° C.) solution of Copper (1) Bromide (4.66 g, 32.5 mmol) in 40% HBr (30 mL)). After the addition, the mixture was heated to 80° C. for 1.5 hours. Then the mixture was allowed to cool to ambient temperature. The solid, which had formed in the reaction mixture, was collected by filtration. Then recrystallized from hot EtOAc and Hexanes, after drying, gave a brown crystalline solid, which was titled product (4.576 g; 18.9 mmol). MS (ESI pos. ion) m/z: 243 (M+H). Calc'd Exact Mass for C9H5BrCl: 242.5
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08017601B2 |
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| 출처 데이터셋 | uspto-grants-2011_09 |
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| ORD ID | ord-a7dbc53bee154fc9ac9019b586f9928a |
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| 출처 메모 | uspto-grants-2011_09 |
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