HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → (R)-N-[(1,1-Dimethyl)ethoxycarbonyl]-S-methylcysteine N-methoxy-N-methylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | Boc-cys(ME)-OH | HCID 7018744 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-N-[(1,1-Dimethyl)ethoxycarbonyl]-S-methylcysteine N-methoxy-N-methylamide | HCID 22942147 | — |
Reaction Steps
A solution of Boc-S-methylcysteine (5 g), N,O-dimethylhydroxylamine hydrochloride (2.28 g) and N-hydroxybenzotriazole monohydrate (3.16 g) in tetrahydrofuran (60 ml) was treated with N-methylmorpholine at 0° C. under nitrogen. EDC (4.89 g) was added and the reaction was warmed to RT and stirred for 48 hours. The reaction mixture was concentrated in vacuo, to give a colourless residue which was partitioned between ethyl acetate (100 ml) and 10% citric acid (100 ml). The organic phase was washed with saturated sodium bicarbonate (70 ml) and brine (70 ml), dried (MgSO4), and evaporated to dryness in vacuo to give the title compound as a pale waxy solid (1.16 g, 29%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06090840 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-c8b01705618447b082dcc8c31c571ba6 |
| Source note | uspto-grants-2000_07 |