HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 20254447, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 20254479 | HCID 20254479 | — |
| Reactant | HCID 53855542 | HCID 53855542 | — |
| Product | HCID 20254447 | HCID 20254447 | — |
Reaction Steps
A mixture of 1 g of 3-acetyloxy-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid and 1 g of 2,5-diamino-2-difluoromethylvaleric acid chloride wherein the free amino groups are protected with tert-butoxycarbonyl in 50 ml of ethylacetate is refluxed for 2 hours after which the solvent is removed leaving a residue which is treated with mild acid and chromatographed on silica gel using benzene-acetone as the eluant to give 7-[[2,5-diamino-2-difluoromethylvaleryl]amino]-3-acetyloxymethyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04438270 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-74d0821336264d8494ab38ac033f3d52 |
| Source note | uspto-grants-1984_03 |