HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → benzyloxycarbonyl-L-histidyl-glycine amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Glycinamide hydrochloride | HCID 2723639 | — |
| Reactant | HCID 178523877 | HCID 178523877 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | benzyloxycarbonyl-L-histidyl-glycine amide | HCID 178514040 | — |
Reaction Steps
Na -t-butyloxycarbonyl-Nim -benzyloxycarbonyl-L-histidine was dissolved in tetrahydrofuran (THF) and neutralized with one equivalent of N-methylmorpholine. It was then coupled with glycinamide hydrochloride using isobutyl chloroformate and N-methylmorpholine. After two hours at -20° C. and an additional hour at ambient temperature, the reaction was quenched with 2N aqueous potassium bicarbonate. This product was extracted into ethyl acetate, washed with 1M aqueous citric acid, and saturated sodium bicarbonate. The organic phase was dried over anhydrous sodium sulfate. Filtration and evaporation gave Na -t-butyloxycarbonyl-Nim -benzyloxycarbonyl-L-histidyl-glycine amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05118665 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-d3d0f0ba26784da8bc79687d4d6c20f0 |
| Source note | uspto-grants-1992_06 |