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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 364727생성일: 2026년 10월 26일

6-Aminopenicillanic acid → 3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid

https://huagongshe.com/reaction/364727

반응식

참여 물질

역할이름HCID투입량
반응물6-Aminopenicillanic acidHCID 11082—
반응물1-PiperidinecarboxaldehydeHCID 17429—
반응물DiisopropylethylamineHCID 81531—
용매ChloroformHCID 6212—
생성물3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acidHCID 1231404722,371.5%

반응 단계

A mixture of 4-[3-(1H-imidazol-1-yl)propyl]-piperidine (1.5 g, 0.0078M) and dimethylformamide dimethylacetal (10 ml) was heated at 100° C. for 16 hrs. The excess of dimethylformamide dimethylacetal was removed to give 4-[3-(1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde dimethylacetal. To the mixture of 6-aminopenicillanic acid (1.16 g, 0.0053M) and diisopropylethylamine (1.03 ml) in dry CHCl3 (9 ml) was added the above piperidinecarboxaldehyde in CHCl3 (5 ml) at 0° C. and stirred at that temperature for 1 hr, then at room temperature for 3 hrs. After the reaction, the solvent was removed and the residue dissolved in water (40 ml). The aqueous solution, washed with diethyl ether, was adjusted to pH 3 with dilute aqueous HCl and purified on Sephadex LH 20 column to give [2S-(2alpha,5alpha,6beta)]-6-[[4-[3-(1 H-imidazol-1-yl)propyl]-1-piperidinyl]methylene]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 1.2 mole hydrochloride monohydrate (0.87 g, 39% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04605744
출처 데이터셋uspto-grants-1986_08
ORD IDord-1880e61f9cc346b8afcdc0f324039003
출처 메모uspto-grants-1986_08