HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → Boc-(D)Ala-Gly-OBzl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | BOC-D-alanine | HCID 637606 | — |
| Reactant | HCID 124082031 | HCID 124082031 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Boc-(D)Ala-Gly-OBzl | HCID 15567200 | — |
Reaction Steps
1.9 g of Boc-(D)Ala-OH and 1.3 ml of N-ethylmorpholine are dissolved in 50 ml of absolute tetrahydrofuran and 1.3 ml of chloroformic acid iso-butyl ester added dropwise at a temperature of -15°. After 5 minutes, a solution of 3.4 g of glycine-benzylester-tosylate and 1.3 ml of N-ethylmorpholine in 50 ml of DMF is added. After 1 hour's stirring at -10°, the reaction mixture is evaporated and the residue taken up in acetic acid. The solution is repeatedly washed with dilute citric acid and potassium bicarbonate. The title compound is crystallised from ether. M.P. 88°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04438103 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-dc6f42968a364588b273152e97690ea0 |
| Source note | uspto-grants-1984_03 |