HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(2-methoxycarbonylethyl)phenyl)-4-ethylthiobutanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Reactant | Methyl 2-(4-aminophenyl)propanoate hydrochloride | HCID 15580485 | — |
| Reactant | HCID 178446879 | HCID 178446879 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(2-methoxycarbonylethyl)phenyl)-4-ethylthiobutanamide | HCID 54278915 | — |
Reaction Steps
The procedure described in Example 177 was repeated, except that (RS)-2-(4-chlorobenzenesulfonylamino)-4-ethylthiobutanoic acid (1.0 g) and methyl 4-aminophenylpropionate hydrochloride (638.4 mg) were condensed in chloroform (30 ml) in the presence of triethylamine (1.4 ml) and 1-methyl-2-chloropyridinium iodide (907.5 mg) to obtain (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(2-methoxycarbonylethyl)phenyl)-4-ethylthiobutanamide (374 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05650428 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-58f35a1b842649e1bad0770aefcbe237 |
| Source note | uspto-grants-1997_07 |