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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 6-Aminopenicillanic acid | HCID 11082 | — |
| 반응물 | 1-Piperidinecarboxaldehyde | HCID 17429 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid | HCID 12314047 | 22,371.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04605744 |
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| 출처 데이터셋 | uspto-grants-1986_08 |
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| ORD ID | ord-1880e61f9cc346b8afcdc0f324039003 |
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| 출처 메모 | uspto-grants-1986_08 |
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