HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → HCID 54170884, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-carbobenzyloxyalanine | HCID 736104 | — |
| Reactant | HCID 68125460 | HCID 68125460 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54170884 | HCID 54170884 | — |
Reaction Steps
To a solution of 0.005 mole of carbobenzyloxyalanine in 100 ml of dry tetrahydrofuran which has been cooled to -20° to -30° is added 1 ml of N-methylmorpholine and then 1 ml of isobutyl-chloroformate. After stirring for 10 minutes there is added 0.005 mole of alanylprolyl-2-azaalanine ethyl ester trifluoroacetic acid salt, 60 ml of chloroform and 1 ml of N-methylmorpholine. The reaction mixture is stirred overnight at room temperature, concentrated in vacuo, the residue treated with ethylacetate and the insoluble material removed by filtration. The filtrate is concentrated in vacuo and the residue chromatographed on a silica gel. Elution with ethyl acetate gives carbobenzyloxyalanylalanylprolyl-2-azaalanine ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04029772 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-56733b071fa74516bc965fee20d5e578 |
| Source note | uspto-grants-1977_06 |