HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → N-t-butoxycarbonyl-L-tyrosylglycylglycine benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Glycyl-glycine benzyl ester hydrochloride | HCID 13996146 | — |
| Reactant | N-t-butoxycarbonyl-L-tyrosine 2,3,5-trichlorophenyl ester | HCID 54469426 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-t-butoxycarbonyl-L-tyrosylglycylglycine benzyl ester | HCID 10624762 | — |
Reaction Steps
A solution of 4.4 parts glycylglycine benzyl ester hydrochloride, 9.1 parts N-t-butoxycarbonyl-L-tyrosine 2,3,5-trichlorophenyl ester and 1.8 parts N-methylmorpholine in 150 parts methylene chloride is stirred overnight at room temperature. The solvent is then removed by evaporation under reduced pressure. The crude material is subjected to low-pressure column chromatography on silica gel to afford N-t-butoxycarbonyl-L-tyrosylglycylglycine benzyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04092304 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-52d5a1b262c64ca1b274c4f94cea28ae |
| Source note | uspto-grants-1978_05 |