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4-[6-Bromo-2-(oxetan-3-yloxy)-1,3-benzodiazol-1-yl]pyrimidin-2-amine → 4-[6-bromo-2-(2-methoxyethoxy)-1H-1,3-benzodiazol-1-yl]pyrimidin-2-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-[6-Bromo-2-(oxetan-3-yloxy)-1,3-benzodiazol-1-yl]pyrimidin-2-amine | HCID 68181588 | — |
| 溶媒 | 2-Methoxyethanol | HCID 8019 | — |
| 生成物 | 4-[6-bromo-2-(2-methoxyethoxy)-1H-1,3-benzodiazol-1-yl]pyrimidin-2-amine | HCID 68181613 | — |
反応手順
The title compound was prepared by the procedure described for the synthesis of 4-[6-bromo-2-(oxetan-3-yloxy)-1H-1,3-benzodiazol-1-yl]pyrimidin-2-amine, by replacing oxetan-3-ol with 2-methoxyethanol: 1H NMR (500 MHz, DMSO) delta 3.31 (3H, s), 3.83-3.72 (2 H, m), 4.77-4.61 (2H, m), 7.02 (1H, d, J=5.5 Hz), 7.12 (2H, s), 7.48-7.33 (2H, m), 8.38 (1H, d, J=5.5 Hz), 8.45 (1H, d, J=1.8 Hz); LC-MS: m/z=+364/366 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08901313B2 |
| 出典データセット | uspto-grants-2014_12 |
| ORD ID | ord-00321bb0dd6647748901bfc9fb3104b4 |
| 出典メモ | uspto-grants-2014_12 |