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Isatoic Anhydride → 2-amino-N-(2-hydroxyethoxy)benzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Isatoic Anhydride | HCID 8359 | — |
| 反応物 | 2-(Aminooxy)ethanol hemisulfate | HCID 131730924 | — |
| 生成物 | 2-amino-N-(2-hydroxyethoxy)benzamide | HCID 86655145 | 66.6% |
反応手順
1H-3,1-benzoxazine-2,4-dione (320 mg, 1.96 mmol) and 2-(aminooxy)ethanol hemisulfate (990 mg, 3.92 mmol) were reacting using the procedure of example 15.07, starting material. The crude product was purified by flash chromatography on silica gel eluting with 0 to 80% EtOAc in DCM. The solvent was evaporated to dryness to afford 2-amino-N-(2-hydroxyethoxy)benzamide (256 mg, 66.5%) as a pale yellow oil which solidified on standing. NMR Spectrum: (DMSOd6) 3.57-3.64 (m, 2H), 3.85-3.92 (m, 2H), 4.75 (bs, 1H), 6.27 (bs, 2H), 6.49 (dd, 1H), 6.71 (d, 1H), 7.15 (ddd, 1H), 7.34 (dd, 1H), 11.39 (bs, 1H); Mass spectrum: MH+ 197
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08569298B2 |
| 出典データセット | uspto-grants-2013_10 |
| ORD ID | ord-8d9b298418e94afd8b991bd758e653d0 |
| 出典メモ | uspto-grants-2013_10 |