참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzenepropanoic acid, 3-bromo-3-oxo-, ethyl ester | HCID 179368 | — |
| 반응물 | 4-Nitro-1,2-phenylenediamine | HCID 5111791 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | HCID 71284241 | HCID 71284241 | 39.5% |
반응 단계
To a stirred solution of 4-nitrobenzene-1,2-diamine 2 (1.0 g, 6.53 mmol) in acetic acid (20 mL) was added ethyl 3-(3-bromophenyl)-3-oxopropanoate 1 (1.75 g, 6.53 mmol) at RT under inert atmosphere. The resulting reaction mixture was heated to 110° C. and stirred for 12 h. After complete consumption of the starting material (by TLC), the reaction mixture was cooled to RT and diluted with water (100 mL) and extracted with EtOAc (3×50 mL). The combined organic extracts were dried over anhydrous Na2SO4 and concentrated under reduced pressure and the obtained crude was purified by silica gel column chromatography (eluent: 25% EtOAc/Hexane) to afford compound 3 (0.91 g, 39.5%) as yellow solid. 1H NMR (500 MHz, DMSO-d6): δ 10.91 (bs, 1H), 8.25 (s, 1H), 8.09-8.01 (m, 3H), 7.82 (d, J=6.4 Hz, 1H), 7.68 (d, J=7.6 Hz, 1H), 7.57-7.48 (m, 1H), 3.67 (s, 2H). MS (ESI): 361 [M+1]+
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09193710B2 |
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| 출처 데이터셋 | uspto-grants-2015_11 |
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| ORD ID | ord-e24cf15447444fef94a73423e83a53ac |
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| 출처 메모 | uspto-grants-2015_11 |
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