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Methyl bromoacetate → [4-(3-Benzo[d]isoxazolylimino)-1-(4H)-pyridinyl]-acetic acid methyl ester hydrobromide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl bromoacetate | HCID 60984 | — |
| 反応物 | 1,2-Benzisoxazol-3-amine, N-4-pyridinyl- | HCID 9837219 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | [4-(3-Benzo[d]isoxazolylimino)-1-(4H)-pyridinyl]-acetic acid methyl ester hydrobromide | HCID 70280625 | 70% |
反応手順
A mixture of 3-(4-pyridinylamino)-1,2-benzisoxazole (0.9 g, 4.3 mmol) and methyl bromoacetate (0.44 mL, 1.1 eq) in acetonitrile (25 mL) was heated at reflux for one hour. The mixture was then allowed to cool to room temperature and the precipitated product was collected by filtration. The white solid was washed with diethyl ether and dried under vacuum to provide the title compound (1.1 g, 70%), mp 235-236° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05728717 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-dc610c599a6a47cbbab5dcc6ac8c553a |
| 出典メモ | uspto-grants-1998_03 |