HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → Acetylalanylalanylprolyl-2-azaalanyl-DL-lactamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Acetylalanylalanylproline | HCID 12895631 | — |
| Reactant | 2-Azaalanyl-DL-lactamide | HCID 131710979 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Acetylalanylalanylprolyl-2-azaalanyl-DL-lactamide | HCID 131710981 | — |
Reaction Steps
Acetylalanylalanylproline (2 mmole) and N-methylmorpholine (2 mmole) are dissolved in dry tetrahydrofuran (200 ml) and cooled to -20° to -25°. Isobutyl chloroformate (2 mmole) is added, and the mixture is stirred at -20° for 10 minutes. A solution of 2-azaalanyl-dl-lactamide (2 mmole) in tetrahydrofuran (10 ml) is added dropwise, and the mixture is allowed to warm to room temperature over a period of 2 hours and stirred for a further 3 hours. The precipitate is filtered off and the filtrate is evaporated to dryness. Chromatography of the residue on silica gel (70 gm) and elution with 18% methanol in chloroform gives acetylalanylalanylprolyl-2-azaalanyl-dl-lactamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064236 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-e55175b823134fe5ace7da416d5ad15d |
| Source note | uspto-grants-1977_12 |