참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-(Thiophen-3-yl)propanedioic acid | HCID 88782 | — |
| 반응물 | Disodium | HCID 141233 | — |
| 반응물 | HCID 178431949 | HCID 178431949 | — |
| 생성물 | HCID 178431935 | HCID 178431935 | 67% |
반응 단계
(2.69 mmole) of 2-(3-thienyl)malonic acid (British Pat. No. 1,125,557) with 645 mg. (2.69 mmole) of 6-amino-2,2-dimethyl-3-(5-tetrazolyl)penam, according to the procedure of Example CXLVII, affords 810 mg, (67% yield) of 6-(2-carboxy-2-[3-thienyl]acetamido)-2,2-dimethyl-3-(5-tetrazolyl)penam as its disodium salt. The infrared spectrum of the product KBr disc) shows absorptions at 1775 cm-1 (β-lactam), 1670 cm-1 (amide I), 1620 cm-1 (carboxylate) and 1525 cm-1 (amide II). The NMR spectrum (D2O) shows absorptions at 7.80-7.00 ppm (multiplet, thienyl hydrogens), 5.88 ppm (doublet, C-6 hydrogen), 5.65 ppm (doublet of doublets, C-5 hydrogen), 5.40 ppm (doublet, C-3 hydrogen), 1.60 ppm (doublet, C-2 methyl hydrogens) and 1.00 ppm doublet, C-2 methyl hydrogens).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04143039 |
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| 출처 데이터셋 | uspto-grants-1979_03 |
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| ORD ID | ord-578679d2ee8844e3b240df71b2741e70 |
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| 출처 메모 | uspto-grants-1979_03 |
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