Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Potassium | HCID 5462222 | — |
| 반응물 | Cefuroxime | HCID 5479529 | — |
| 반응물 | Bromomethyl 3-methylbutanoate | HCID 20461839 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 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 | — |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04446317 |
| 출처 데이터셋 | uspto-grants-1984_05 |
| ORD ID | ord-5b20fdeb2ec84f16ac26925f939f7bc5 |
| 출처 메모 | uspto-grants-1984_05 |