HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 87421969, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bistrimethylsilylacetamid | HCID 11708267 | — |
| Reactant | HCID 49818931 | HCID 49818931 | — |
| Reactant | HCID 87420773 | HCID 87420773 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 87421969 | HCID 87421969 | — |
Reaction Steps
0.5 g of (6R, 7R)-7-amino-3[E-(R)-1′-(5-methyl-2-oxo-[1,3]-dioxol-4-ylmethoxycarbonyl)-2-oxo-[1,3′]bipyrrolidinyl-3-ylidenemethyl]-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid were dissolved in 20 ml of dichloromethane at 0°. 0.7ml of bis(trimethylsilyl)acetamide were then added and 0.46 g of 2-trityloxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)-acetic acid chloride hydrochloride (J. Antibiotics 37:557-571, 1984) were metered in portions. The mixture was poured onto 15 ml of water/15 ml of MeOH and the phases were separated. The water phase was washed once again with 15 ml of dichloromethane and the combined organic phases were dried over sodium sulfate and concentrated in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096610B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-3f5ea41c5554470181f238d1b33f9255 |
| Source note | uspto-grants-2015_08 |