HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 22844256, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | N-(tert-Butoxycarbonyl)-3-[(triphenylmethyl)sulfanyl]-D-valine | HCID 22844255 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22844256 | HCID 22844256 | 97.2% |
Reaction Steps
To the solution of N-t-butoxycarbonyl-S-trityl-D-penicillamine (A-2) (6.0 g) in dimethylformamide (40 ml), were added methyl iodide (1.5 ml) and potassium hydrogencarbonate (2.4 g), and the mixture was stirred for 14 hours. To the reaction mixture was added ice-water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and then with saturated saline, and dried over magnesium sulfate. The solvent was evaporated off under reduced pressure, to give N-t-butoxycarbonyl-S-trityl-D-penicillamine methyl ester (6.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05116861 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-0fe72926178d4e1d915d96f3657ab157 |
| Source note | uspto-grants-1992_05 |