참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methane | HCID 297 | — |
| 반응물 | Ethylmorpholine | HCID 7525 | — |
| 반응물 | 2-Bromo-3-nitrobenzoic acid | HCID 68452 | — |
| 반응물 | 5-Aminoquinoxaline | HCID 85494 | — |
| 용매 | Ammonia | HCID 222 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | 3-Nitro-(quinoxalinylamino)benzoic acid | HCID 18545444 | 42% |
반응 단계
A mixture of 5-aminoquinoxaline (1.0 g, 6.89 mmol), 2-bromo-3-nitrobenzoic acid (4.0 g, 13.78 mmol), Cu/CuI (catalytic) and N-ethylmorpholine (5 mL) in isopropanol (5 mL) was heated at 65-70° C. overnight. The mixture was then dissolved in aqueous ammonia, treated with charcoal/Celite, and filtered. The filtrate was acidified with conc. HCl, and the resulting precipitate was collected while the mixture was still warm and washed with water (to remove unreacted 2-bromo-3-nitrobenzoic acid). It was then dried and chromatographed on silica gel, eluting with CH2Cl2/MeOH (19:1), to give 3-nitro-(quinoxalinylamino)benzoic acid (0.9 g, 42%): mp (MeOH) 232-237° C.; 1H NMR [(CD3)2SO] δ 6.92-6.97 (m, 1 H, ArH), 7.30 (t, J=8.0 Hz, 1 H, ArH), 7.62-7.66 (m, 2 H, 2xArH), 8.23 (dd, J=8.2, 1.6 Hz, 1 H, ArH), 8.29 (dd, J=7.8, 1.6 Hz, 1 H, ArH), 8.97 (d, J=1.7 Hz, 1 H, H-2′ or H-3′), 9.03 (d, J=1.9 Hz, 1 H, H-2′ or H-3′), 10.73 (br s, 1 H, NH), 13.8 (br s, 1 H, CO2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06552021B2 |
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| 출처 데이터셋 | uspto-grants-2003_04 |
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| ORD ID | ord-86d5a59d56cc4c9c93605e5cfd06affe |
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| 출처 메모 | uspto-grants-2003_04 |
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