HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → HCID 54230031, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Methyl 2-bromopropionate | HCID 95576 | — |
| Reactant | L-Leucine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1) | HCID 6451312 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54230031 | HCID 54230031 | — |
Reaction Steps
Leucine benzyl ester para-toluene sulphonic acid salt (113 g) in dry acetonitrile (800 ml) was treated with methyl 2-bromopropionate (62.7 ml) and N-methyl morpholine (100 ml) under reflux for 16 h. The reaction mixture was concentrated in vacuo and the residue in ethyl acetate washed with brine, dried (Na2SO4) and evaporated. Chromatography of the resulting oil on silica in 1:4 ethyl acetate-hexane gave N-[1-(R)-methoxycarbonylethyl]-L-leucine benzyl ester (45 g) as the faster running fraction. This material was treated exactly as described above in Example 2 to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04568666 |
| Source dataset | uspto-grants-1986_02 |
| ORD ID | ord-cd6b7e2fd21e41fbb5f672d71211e481 |
| Source note | uspto-grants-1986_02 |