HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653272Generated: October 28, 2026
HCID 86740397, compound → HCID 140340256, compound
https://huagongshe.com/reaction/653272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86740397 | HCID 86740397 | — |
| Reactant | HCID 140345753 | HCID 140345753 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 140340256 | HCID 140340256 | — |
Reaction Steps
To a solution of 221 mg of sodium cis-3[2-(2-chloroacetamido-4-thiazolyl)-(Z)-2-methoxyiminoacetamido]-4-[2-(2-chloroacetamido-4-thiazolyl)-(Z)-2-methoxyimino-acetoxymethyl]-2-oxoazetidine-1-sulfonate in 10 ml of water is added under ice-cooling 85 mg of sodium monomethyldithiocarbamate with stirring. The mixture is stirred at room temperature for one hour, followed by addition of 40 mg of sodium monomethyldithiocarbamate. The mixture is stirred at room temperature for further one hour. The reaction mixture is washed with ethyl acetate and ether in this order, followed by concentration under reduced pressure. The concentrate is purified by a column chromatography on Amberlite XAD-II, followed by lyophilization to give sodium cis-3-[2-(2-amino-4-thiazolyl)-(Z)-2-methoxyiminoacetamido]-4-[2-(2-amino-4-thiazolyl)-(Z)-2-methoxyiminoacetoxymethyl]-2-oxoazetidine-1-sulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04675397 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-17830d324e044e17b2545929ed21c98a |
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| Source note | uspto-grants-1987_06 |
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