참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 1,4-Benzenediboronic acid | HCID 230478 | — |
| 반응물 | 4,7-dibromo-2-(pyridin-4-yl)-2H-benzo[d][1,2,3]triazole | HCID 86679901 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 1,4-bis(7-bromo-2-(pyridin-4-yl)-2H-benzo[d][1,2,3]triazol-4-yl)benzene | HCID 86679904 | — |
반응 단계
A mixture of Intermediate A (90%, 2.40 g, 6.14 mmol), 1,4-benzenediboronic acid (248 mg, 1.5 mmol), sodium carbonate (530 g, 5 mmol) in water (4 mL), tetrakis(triphenylphosphine)palladium (0) (500 mg, 0.43 mmol), n-butanol (20 mL), and toluene (20 mL) was stirred and heated under argon at 110° C. for 68 hours. The reaction mixture was poured into water (300 mL), treated with 5N NaOH (50 mL), stirred for 1 hour, and extracted with dichloromethane (3×200 mL, low solubility in dichloromethane). The volatiles were removed under reduced pressure, and the residue was chromatographed (silica gel, chloroform/tetrahydrofuran 9:1). The obtained product was triturated with ethyl acetate (30 mL), filtered off and dried in a vacuum oven to give 1,4-bis(7-bromo-2-(pyridin-4-yl)-2H-benzo[d][1,2,3]triazol-4-yl)benzene (Intermediate G), yellow crystals, 610 mg (purity 80%, yield 65%). 1H NMR (400 MHz, CDCl3): δ 8.86 (m, 4H, pyridine), 8.39 (m, 4H, pyridine), 8.26 (s, 4H, benzotriazole), 7.79 (d, J=7.7 Hz, 2H, benzene), 7.62 (d, J=7.7 Hz, 2H, benzene).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09382424B2 |
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| 출처 데이터셋 | uspto-grants-2016_07 |
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| ORD ID | ord-9255c0789fcb4f03a16a9e677ecb0aeb |
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| 출처 메모 | uspto-grants-2016_07 |
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