HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → L-Pyroglutamyl-4-aminobutyric acid amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | 4-Aminobutanamide | HCID 18615 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 2,4,5-Trichlorophenyl 5-oxo-L-prolinate | HCID 111108 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | L-Pyroglutamyl-4-aminobutyric acid amide | HCID 86735131 | — |
Reaction Steps
3.9 g (12.65 mmols) of L-pyroglutamic acid 2,4,5-trichlorophenyl ester were added to a solution of 1.76 g (12.9 mmols) 4-amino butyric acid amide and 1.72 g (12.75 mmols) of 1-hydroxybenzotriazole and 1.65 ml of N-ethylmorpholine in 40 ml of dimethyl formamide. The solution was allowed to stand for 1 hour at room temperature. It was concentrated and triturated with ether. The substance was suction-filtered and chromatographed in methanol/water (1:1) through Serdolit Blau. The eluate was concentrated and the residue was triturated with ether and suction-filtered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04053588 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-99c8a129abd1453e801d533d1ba8d348 |
| Source note | uspto-grants-1977_10 |