HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → HCID 22844258, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | HCID 22844257 | HCID 22844257 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22844258 | HCID 22844258 | 102.2% |
Reaction Steps
To the solution of N-t-butoxycarbonyl-S-trityl-L-penicillamylglycine ethyl ester (B-2) (4.5 g) and 2,6lutidine (2.8 ml) in dichloromethane (100 ml), was added dropwise at 0° C. the solution of trimethylsilyl trifluoromethanesulfonate (3.9 ml), and the mixture was stirred for 1 hour while the temperature was gradually returned to the room temperature. To the reaction mixture was added ice-water, and the organic layer was washed with 1N-hydrochloric acid, water, an aqueous solution of sodium hydrogencarbonate, water, and saturated saline, in this order, and dried over magnesium sulfate. The solvent was evaporated off under reduced pressure, to give S-trityl-L-penicillamylglycine ethyl ester (3.8 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05116861 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-d1a6480ba59a42bfa575cd52511f2274 |
| Source note | uspto-grants-1992_05 |