HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethyl cis-4-[[(4-chlorophenyl)carbonyl]amino]-5-oxo-1-phenyl-3-pyrrolidinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | Ethyl 4-amino-5-oxo-1-phenyl-3-pyrrolidinecarboxylate | HCID 19023548 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl cis-4-[[(4-chlorophenyl)carbonyl]amino]-5-oxo-1-phenyl-3-pyrrolidinecarboxylate | HCID 67794583 | 69.3% |
Reaction Steps
To a solution of p-chlorobenzoyl chloride (247 mg, 1.41 mmol) in CH2Cl2 (4 ml) was added a solution of aminopyrrolidinone of Example S (350 mg, 1.41 mmol) and triethylamine (0.4 ml, 2.82 mmol) in CH2Cl2 (4 ml) and the resulting solution was stirred for 18 h at room temperature. Concentration in vacuo gave an oil which was chromatographed on silica gel eluting with 5/95 EtOH/CH2Cl2 to give the title compound (378 mg, 68%) as a solid. Anal calcd for C20H19N2O4Cl; C, 62.10; H, 4.95; N, 7.24. Found: C, 62.07; H, 5.05; N, 7.18. MS calcd for C20H19N2O4Cl 386, found 386. DSC=215.2°-216.8° C. at 144.3 J/g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05314886 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-27c0640d5f244a389294d6499697409d |
| Source note | uspto-grants-1994_05 |