HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-((Acetyloxy)methyl)-7-amino-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid → HCID 21493851, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-((Acetyloxy)methyl)-7-amino-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid | HCID 13729 | — |
| Reactant | HCID 88807898 | HCID 88807898 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21493851 | HCID 21493851 | — |
Reaction Steps
A mixture of 1 g of 3-[(acetyloxy)methyl]-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid and 1.2 g of 2-chloromethyl-4-methoxymandelic acid chloride in 200 ml of ethyl acetate is refluxed for 50 minutes after which the solvent is removed under high vacuum. The resulting product is chromatographed on silica gel using benzene-actone as the eluant. The product obtained is triturated with ether to give 3-[(acetyloxy)methyl]-7-[[2-[2-(chloromethyl)-4-methoxyphenyl]-2-hydroxyacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. M.P. 140°-142°C (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03948904 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-5130300569f6462d849f77d6a4cd3685 |
| Source note | uspto-grants-1976_04 |