HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448395Generated: November 3, 2026
HCID 20381532, compound → HCID 178431932, compound
https://huagongshe.com/reaction/1448395
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 20381532 | HCID 20381532 | — |
| Reactant | HCID 178431949 | HCID 178431949 | — |
| Product | HCID 178431932 | HCID 178431932 | 63% |
Reaction Steps
(2.0 mmole) of 5-indanyl 2-phenylmalonate with 480 mg. (2.0 mmole) of 6-amino-2,2-dimethyl-3-(5-tetrazolyl)penam, according to the procedure of Example CXLVII affords 680 mg. (63% yield) of 6-(2-[5-indanyloxycarbonyl]-2-phenylacetamido)-2,2-dimethyl-3-(5-tetrazolyl)penam as its sodium salt. The infrared spectrum (KBr disc) of the product shows absorption bands at 1780 cm-1 (β-lactam), 1705 cm-1 (ester), 1680 cm-1 (amide I) and 1565 cm-1 (amide II). The NMR spectrum (D2O) shows absorption bands at 7.80-6.80 ppm (multiplet, aromatic hydrogens), 5.70 ppm (multiplet, C-5 and C-6 hydrogens), 5.25 ppm (doublet, C-3 hydrogen), 2.60-2.00 ppm (multiplet, C-1 and C-3 indanyl hydrogens), 2.00-1.80 ppm (multiplet, C-2 indanyl hydrogens), 1.35 ppm (doublet, C-2 methyl hydrogens) and 0.90 ppm (doublet, C-2 methyl hydrogens).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04179511 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-1bea0b05850342fb98317831a2ca7def |
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| Source note | uspto-grants-1979_12 |
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