化工社化工社 化学情報印刷レポート · 研究参考用
6-Amino-o-cresol → HCID 178423983、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 6-Amino-o-cresol | HCID 413657 | — |
| 反応物 | HCID 178424098 | HCID 178424098 | — |
| 反応物 | HCID 178480983 | HCID 178480983 | — |
| 生成物 | HCID 178423983 | HCID 178423983 | — |
反応手順
Cis-N2-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}phenyl)-7-methyl-1,3-benzoxazol-2-amine was prepared from cis-3-(4-aminophenyl)-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-4-amine (0.100 g, 0.245 mmol) and 2-amino-6-methylphenol (0.030 g, 0.245 mmol) in a manner similar to that used in the synthesis of cis-N2-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}phenyl)-4-methyl-1,3-benzoxazol-2-amine (PH4052419F). The compound was formed as an off-white solid (0.018 g, 14%): RP-HPLC (25 to 100% CH3CN in 0.1 N aqueous ammonium acetate over 10 min at 1 mL/min using a Hypersil HS C18, 100 Å, 5 μm, 250×4.6 mm column) tr=7.37 min., 85%; m/z 539 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06921763B2 |
| 出典データセット | uspto-grants-2005_07 |
| ORD ID | ord-162f0e8cd1644fdfb1ecb163c9c32e5a |
| 出典メモ | uspto-grants-2005_07 |