HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → Acetylalanylalanylleucine benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-Acetyl-L-alanine | HCID 88064 | — |
| Reactant | HCID 68124634 | HCID 68124634 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Acetylalanylalanylleucine benzyl ester | HCID 54388809 | — |
Reaction Steps
To a stirred solution of acetylalanine (0.03 mole) and N-methylmorpholine (0.03 mole) in dry tetrahydrofuran (200 ml) at -20° to -25° is added isobutyl chloroformate (0.03 mole). After 10 minutes, a suspension of the crude alanylleucine benzyl ester hydrochloride (0.03+ mole) and N-methylmorpholine (0.04 mole) in tetrahydrofuran (25 ml) is added in portions over 1/2 hour. The mixture is allowed to warm to room temperature over a period of 2 hours and stirred overnight. The reaction mixture is evaporated to dryness and the residue is purified by chromatography on silica gel (200 gm) and elution with 10% methanol in chloroform to give acetylalanylalanylleucine benzyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064236 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-d1bd7cc0dc764d9e8254ab55b64eaa2c |
| Source note | uspto-grants-1977_12 |