化工社化工社 化学情報印刷レポート · 研究参考用
Potassium → 3-methylbutanoyloxymethyl (6R,7R)-3-(carbamoyloxymethyl)-7-[[(2Z)-2-(furan-2-yl)-2-methoxyiminoacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium | HCID 5462222 | — |
| 反応物 | Cefuroxime | HCID 5479529 | — |
| 反応物 | Bromomethyl 3-methylbutanoate | HCID 20461839 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-methylbutanoyloxymethyl (6R,7R)-3-(carbamoyloxymethyl)-7-[[(2Z)-2-(furan-2-yl)-2-methoxyiminoacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | HCID 177714162 | — |
反応手順
Bromomethyl 3-methylbutanoate (1.328 g, 6.7 mmole) was added to a solution of (6R,7R)-3-carbamoyloxymethyl-7-[(Z)-2-(fur-2-yl)-2-methoxyiminoacetamido]ceph-3-em-4-carboxylic acid, potassium salt (2.772 g, 6 mmole) in purified N,N dimethylformamide (18 ml). The mixture was allowed to react for 15 minutes and was then worked up as described in Example 4 to give the slightly impure title compound (2.809 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04446317 |
| 出典データセット | uspto-grants-1984_05 |
| ORD ID | ord-5b20fdeb2ec84f16ac26925f939f7bc5 |
| 出典メモ | uspto-grants-1984_05 |