HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 19833167, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Glycine ethyl ester, hydrochloride | HCID 2723640 | — |
| Reactant | HCID 19833168 | HCID 19833168 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19833167 | HCID 19833167 | — |
Reaction Steps
6.00 g (0.015 mol) of 2-[4-(4-acetamidobutyramido)butyryl]-5-chlorohydrocinnamic acid and 2.57 g (0.016 mol) of 1,1'-carbonyldiimidazole are stirred at room temperature for 1.5 hours in 60 ml of tetrahydrofuran and 2.22 g (0.016 mol) of ethyl glycinate hydrochloride and 2.2 ml (0.016 mol) of triethylamine are added thereto. After stirring at room temperature for 1 hour, the solution is concentrated, extracted with methylene chloride/water, dried with magnesium sulfate and the solvent is distilled in a vacuum. Chromatography on silica gel with ethyl acetate-ethanol (9:1) and crystallization from methanol-ether gives ethyl N-[2-[4-(4-acetamidobutyramido)butyryl]-5-chlorohydrocinnamoyl]glycinate as white crystals with melting point 94°-96°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04883815 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-c223f7855d2f427983ca5089f526fdbf |
| Source note | uspto-grants-1989_11 |