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1,2-Benzenedicarbonitrile, 4-amino- → HCID 178462398、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2-Benzenedicarbonitrile, 4-amino- | HCID 92529 | — |
| 反応物 | Trimethylaluminum | HCID 16682925 | — |
| 反応物 | HCID 178497884 | HCID 178497884 | — |
| 生成物 | HCID 178462398 | HCID 178462398 | 71% |
反応手順
In the same manner as that described in Example 3(4), a reaction was carried out using commercially available 4-aminophthalonitrile (170 mg, 1.2 mmol), trimethylaluminium (1.1 ml, 1.07M n-hexane solution, 1.2 mmol) and methyl 4-[trans-5-[[(1R,2R)-2-(2,4-difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1,2,4-triazol-1-yl)propyl]thio]-1,3-dioxan-2-yl]benzoate (150 mg, 0.30 mmol), obtained in Example 12(1), and the reaction mixture was treated using a similar procedure to that described in Example 3(4) to afford the title compound (129 mg, yield 71%) as a yellow oil which was recrystallized from ethyl acetate-hexane to give pale yellow powdery crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06653330B2 |
| 出典データセット | uspto-grants-2003_11 |
| ORD ID | ord-111708407deb490b9a820a19078cab2f |
| 出典メモ | uspto-grants-2003_11 |