돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 543530생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/543530

반응식

참여 물질

역할이름HCID투입량
반응물PotassiumHCID 5462222—
반응물CefuroximeHCID 5479529—
반응물Bromomethyl 3-methylbutanoateHCID 20461839—
용매DimethylformamideHCID 6228—
생성물3-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-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04446317
출처 데이터셋uspto-grants-1984_05
ORD IDord-5b20fdeb2ec84f16ac26925f939f7bc5
출처 메모uspto-grants-1984_05