HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349559Generated: October 30, 2026
HCID 141601005, compound → HCID 141601007, compound
https://huagongshe.com/reaction/349559
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 141601005 | HCID 141601005 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 141601007 | HCID 141601007 | 38.6% |
Reaction Steps
A solution of 7β-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(1-carboxy-1-methylethoxyimino)acetamido]-3-[3-(formamidomethyl)-4,5,6,7-tetrahydro-1-pyrazolo[1,5-a]pyrimidinio]methyl-3-cephem-4-carboxylate (130 mg) in 10% aqueous hydrochloric acid (4.36 ml) was stirred at room temperature for 6 hours. The reaction mixture was purified by preparative HPLC utilizing ODS column. The eluate containing a desired product was concentrated to about 30 ml in vacuo. The concentrate was adjusted to about pH 3 with concentrated hydrochloric acid and chromatographed on Diaion® HP-20 (Mitsubishi Chemical Corporation) eluting with 30% aqueous 2-propanol. The eluate was concentrated to about 30 ml in vacuo and lyophilized to give 7β-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(1-carboxy-1-methylethoxyimino)acetamido]-3-(3-aminomethyl-4,5,6,7-tetrahydro-1-pyrazolo[1,5-a]pyrimidinio)methyl-3-cephem-4-carboxylate (48 mg) as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07179801B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-00966f5951e14feea7101aeed20cc7de |
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| Source note | uspto-grants-2007_02 |
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