HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → Boc-Tyr-(D)Ala-Gly-Phe methioninol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Boc-tyr-D-ala-gly-OH | HCID 7272028 | — |
| Reactant | H-Phe methioninol trifluoroacetate | HCID 131712175 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Boc-Tyr-(D)Ala-Gly-Phe methioninol | HCID 131712172 | — |
Reaction Steps
4.1 g of Boc-Tyr-(D)Ala-Gly-OH and 1.1 ml of N-methyl-morpholine are dissolved in 50 ml of absolute tetrahydrofuran and 1.0 ml of chloroformic acid ethyl ester added dropwise at -15°. After 5 minutes, a solution of 4.0 g of H-Phe-methioninol trifluoroacetate and 1.2 ml of N-methylmorpholine in 50 ml of DMF is added. After 1 hour's stirring at 0°, the reaction mixture is evaporated and the residue taken up in acetic acid. The solution is repeatedly washed with 10% phosphoric acid and 1 N sodium bicarbonate. After evaporation of the acetic esters, the residue is crystallised from methanol/ether. M.P. 158°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04261888 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-b8f3daf14e334c958628ebe0f1daf6f1 |
| Source note | uspto-grants-1981_04 |