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1H-Indazol-6-amine → 2-[(4-t-Butylbenzoyl)amino]-N-(6-indazolyl)-5-nitrobenzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1H-Indazol-6-amine | HCID 81423 | — |
| 反応物 | 2-(4-Tert-butylphenyl)-6-nitro-3,1-benzoxazin-4-one | HCID 385599 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 2-[(4-t-Butylbenzoyl)amino]-N-(6-indazolyl)-5-nitrobenzamide | HCID 18373189 | 42.2% |
反応手順
To a stirring solution of 6-nitro-2-[4-t-butylphenyl]-4H-3,1-benzoxazin-4-one (1.5 g, 4.62 mmol) in toluene (25 mL) was added 6-aminoindazole (560 mg, 4.2 mmol) and the solution was heated to reflux. After about 24 h, the solution was cooled, filtered and the solid was washed with diethyl ether. The product was then chromatographed over silica gel, eluting with 25% ethyl acetate/hexanes. The product containing fractions were combined and concentrated in vacuo to give 810 mg (42%) of pale yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06372759B1 |
| 出典データセット | uspto-grants-2002_04 |
| ORD ID | ord-afe226187cf645d8a41ba8893b54973c |
| 出典メモ | uspto-grants-2002_04 |