HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Benzylglycine ethyl ester → HCID 21463502, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Benzylglycine ethyl ester | HCID 80908 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 3-(4,5,7-Trifluorobenzothiazol-2-yl)propionic acid | HCID 21463529 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21463502 | HCID 21463502 | 78% |
Reaction Steps
To methylene chloride (10 ml) was added 3-(4,5,7-trifluorobenzothiazol-2-yl)propionic acid (522 mg, 2 mmol) obtained in Example 3-i), WSC.HCl (422 mg, 2.2 mmol) and N-benzylglycine ethyl ester (386 mg, 2 mmol) and the mixture was stirred for 15 hours at room temperature. The reaction mixture was washed with 7% hydrochloric acid and water successively. The organic layer was dried and evaporated. The resulting residue was purified on a silica gel column to give N-benzyl-N-[3-(4,5,7-trifluorobenzothiazol-2-yl)propionyl]-glycine ethyl ester (680 mg, 78%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05700819 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-7897ee35011b4edf81e1bda2a1c1957d |
| Source note | uspto-grants-1997_12 |