HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221172Generated: October 29, 2026
4-Methylmorpholine → HCID 131721608, compound
https://huagongshe.com/reaction/2221172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 10507094 | HCID 10507094 | — |
| Reactant | HCID 10888348 | HCID 10888348 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131721608 | HCID 131721608 | 75.4% |
Reaction Steps
2 g (3.35 mmol) Z-Val-Val-MeVal-Pro-OH (SEQ ID NO: 2) and 0.692 g (3.35 mmol) H-Pro-NHC(CH3)3 were dissolved in 34 ml of dry dichloromethane. After cooling to 0° C., 1.35 ml (12.1 mmol) N-methylmorpholine, 0.114 g (0.84 mmol) HOBt and 0.645 g (3.35 mmol) EDCI were added and the reaction mixture stirred overnight at room temperature. 80 ml dichloromethane were added and the organic phase thoroughly washed with saturated aqueous NaHCO3 solution (3×), water (1×), 5% citric acid (3×) and saturated NaCl solution (1×). The organic phase was dried over sodium sulfate and evaporated to dryness to yield 1.8 g of the product which was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07368528B2 |
|---|
| Source dataset | uspto-grants-2008_05 |
|---|
| ORD ID | ord-e772a3eabde44e30b32ccb3d3456b1f3 |
|---|
| Source note | uspto-grants-2008_05 |
|---|