HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (S)-N-(Phenylmethyl)-2-[[(S)-2-(pivaloyloxyacetyl)-1-pyrrolidinyl]carbonyl]-1-pyrrolidinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Jtp-4819 | HCID 178060 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-N-(Phenylmethyl)-2-[[(S)-2-(pivaloyloxyacetyl)-1-pyrrolidinyl]carbonyl]-1-pyrrolidinecarboxamide | HCID 15389025 | — |
Reaction Steps
Triethylamine (0.59 ml), pivaloyl chloride (0.43 ml) were added, under ice-cooling, to a methylene chloride solution (25 ml) of (S)-2-[[(S)-2-(hydroxyacetyl)-1-pyrrolidinyl]carbonyl]-N-(phenylmethyl)-1-pyrrolidinecarboxamide (1.26 g) obtained in Example 5 and the mixture was stirred for 17 hours. The reaction mixture was poured into 5% potassium hydrogensulfate and extracted with methylene chloride. The extract was washed with saturated sodium hydrogencarbonate and water in order, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (eluent: chloroform-methanol) to give the title compound (1.21 g) (see Table 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05536737 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-7d465bad36c84b768b8f1522c0f5e890 |
| Source note | uspto-grants-1996_07 |