HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → HCID 22844259, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Trifluoromethanesulfonate | HCID 2758875 | — |
| Reactant | HCID 86745855 | HCID 86745855 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22844259 | HCID 22844259 | — |
Reaction Steps
To the solution of tetrabutylammonium N-t-butoxycarbonyl-S-trityl-L-penicillamyl-p-sulfophenylalanine (B-23)(7.5 g) and 2,6-lutidine (3.8 ml) in dichloromethane (100 ml), was added dropwise at 0° C. the solution of trimethylsylyl trifluoromethanesulfonate (5.5 ml), and the mixture was stirred for 1 hour while the temperature was gradually returned to the room temperature. The solvent was evaporated off under reduced pressure and the residue was washed with diethyl ether and acetone, in this order, to give S-trityl-L-penicillamyl-p-sulfophenylalanine (3.lg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05116861 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-cef743b7443849d0ad4c33d8f8523b33 |
| Source note | uspto-grants-1992_05 |