HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → L-Pyroglutamyl-4-aminobutyric acid tert. butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | 2,4,5-Trichlorophenyl 5-oxo-L-prolinate | HCID 111108 | — |
| Reactant | Tert-butyl 4-aminobutanoate hydrochloride | HCID 24750478 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | L-Pyroglutamyl-4-aminobutyric acid tert. butyl ester | HCID 86735130 | — |
Reaction Steps
1.3 ml of N-ethylmorpholine and 3.08 g of L-pyroglutamic acid 2,4,5-trichlorophenyl ester were added to a solution of 1.95 g (10 mmols) of 4-aminobutyric acid tert. butyl ester hydrochloride in 20 ml of dimethylformamide. The solution was left overnight at room temperature. It was concentrated, the residue was dissolved in a mixture of ethyle acetate and water, and the ethyl acetate solution was shaken with sodium bicarbonate solution, KHSO4 -solution and NaCl-solution, dried with Na2SO4 and concentrated. The residue was triturated with petroleum ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04053588 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-3efe0805a99f47fb833d80e4b5e3d2d6 |
| Source note | uspto-grants-1977_10 |