HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 11337051, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyloxycarbonyl-L-proline | HCID 101987 | — |
| Reactant | L-Serine, methyl ester, hydrochloride (1:1) | HCID 2723730 | — |
| Reactant | 1-(p-Chlorobenzenesulfonyloxy)-6-chloro-1,2,3-benzotriazole | HCID 12222841 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11337051 | HCID 11337051 | 79.7% |
Reaction Steps
N-Benzyloxycarbonyl-L-proline (1.25 g), L-serine methyl ester hydrochloride (0.78 g) and triethylamine (1.40 ml) are dissolved in dry chloroform (20 ml) and thereto is added 1-(p-chlorobenzenesulfonyloxy)-6-chloro-1,2,3-benzotriazole (1.72 g) under ice-cooling. After allowing to stand overnight, to the mixture are added water and ethyl acetate. The ethyl acetate layer is washed and dried, and then the solvent is distilled off to give N-(N-benzyloxycarbonyl-L-prolyl)-L-serine methyl ester (1.4 g), melting point: 96°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04242507 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-3cd8063d30fd4c84bc76418944d40333 |
| Source note | uspto-grants-1980_12 |