関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Bromo-5-nitrothiazole | HCID 18211 | — |
| 反応物 | 4-[4-(4-Aminophenyl)phenyl]-2,2-dimethyl-4-oxobutanoic acid | HCID 21985693 | — |
| 溶媒 | 1-Butanol | HCID 263 | — |
| 生成物 | 2,2-Dimethyl-4-{4'-[(5-nitro-1,3-thiazol-2-yl)amino]-1,1'-biphenyl-4-yl}-4-oxobutanoic acid | HCID 11669054 | 10.5% |
反応手順
In a 8-mL screw-cap vial, a mixture of 4-(4′-amino-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoic acid (60 mg, 0.20 mmol) and 2-bromo-5-nitro-1,3-thiazole (63.3 mg, 0.30 mmol) in 4 mL n-butanol was heated at 90° C. overnight. The solvent was removed under reduced pressure. The mixture was dissolved in 5 mL 1:4 MeOH/DMF and purified by reverse-phase HPLC to provide 8.9 mg (10%) of the desired product. 1H NMR (400 MHz, DMSO-d6) δ 11.55 (br s, 1 H), 8.50 (s, 11 H), 7.70–8.05 (m, 8 H), 3.15 (d, 1 H), 1.25 (s, 6 H); LC-MS m/z 426.2 (MH+), ret. time 3.12 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07091228B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-a18740d4bfe14cca8aefbb9921da9aa9 |
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| 出典メモ | uspto-grants-2006_08 |
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