HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383742Generated: November 2, 2026
4-Methylmorpholine → Z-N-Me-Val-N-Me-Tyr(3-tBu)-NH2
https://huagongshe.com/reaction/1383742
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Z-N-Me-Val-N-Me-Tyr(3-tBu)-OH | HCID 131722750 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl chloroformate | HCID 10928 | — |
| Product | Z-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 | HCID 131722751 | — |
Reaction Steps
To a solution of 1.96 g of Z-N-Me-Val-N-Me-Tyr(3-tBu)-OMe in 1,4-dioxane (40 ml), 2 N NaOH (5 ml) was added at room temperature and the mixture was stirred for 2 hours. The reaction mixture was adjusted to pH 3 with dilute hydrochloric acid and extracted with ethyl acetate. The extract was washed with saturated brine and the organic layer was dried with sodium sulfate. The solvent was distilled off under reduced pressure to give Z-N-Me-Val-N-Me-Tyr(3-tBu)-OH. To a solution of this Z-N-Me-Val-N-Me-Tyr(3-tBu)-OH in THF (20 ml), ethyl chloroformate (0.40 ml) and NMM (0.46 ml) were added under cooling with ice and the mixture was stirred for 15 minutes. Subsequently, ammonia gas was bubbled into the reaction mixture for 5 minutes. The solvent was distilled off under reduced pressure and the precipitating salt was filtered off and washed with ethyl acetate. The solvent was distilled off under reduced pressure and the resulting residue was subjected to silica gel column chromatography (eluting solvent; n-hexane:ethyl acetate=2:3) to give Z-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 in the amount of 1.17 g (61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06255285B1 |
|---|
| Source dataset | uspto-grants-2001_07 |
|---|
| ORD ID | ord-6c162120214b404eaacf787832fd716b |
|---|
| Source note | uspto-grants-2001_07 |
|---|