HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → N-(cholest-5-ene-3beta-oxycarbonyl)glycylglycine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Glycylglycine | HCID 11163 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | C28H45ClO2 | HCID 54236888 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(cholest-5-ene-3beta-oxycarbonyl)glycylglycine | HCID 131717552 | 80.8% |
Reaction Steps
Sodium hydrogencarbonate (0.168 g) and tetrahydrofuran (20 ml) were added to a suspension of glycylglycine (0.15 g) in water (20 ml). After tetrahydrofuran (20 ml) and cholesteryl chloroformate (0.898 g) were added to the resulting transparent solution at 0° C., the mixture was stirred for an hour. The reaction mixture was concentrated under reduced pressure and, methanl (10 ml) and chloroform (10 ml) were added to the residue. By filtration, the transparent solution was obtained. The solvent was distilled off to give crude crystals (0.98 g). The crude crystals were then purified by silica gel chromatography to give N-(cholest-5-ene-3β-oxycarbonyl)glycylglycine (0.5 g) as white powders.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05152999 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-c01942f2ad344ee7b3deac1007c75775 |
| Source note | uspto-grants-1992_10 |