HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butoxycarbonylalanine → N-[N-(Dec-4enoyl)-L-alaninyl]-L-phenylalanine Methyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butoxycarbonylalanine | HCID 85082 | — |
| Reactant | L-Phenylalanine, methyl ester | HCID 736234 | — |
| Reactant | Alanylphenylalanine methyl ester | HCID 12988705 | — |
| Product | N-[N-(Dec-4enoyl)-L-alaninyl]-L-phenylalanine Methyl Ester | HCID 54300131 | — |
Reaction Steps
Following General Procedure A and using N-(L-alaninyl)-L-phenylalanine methyl ester (prepared by coupling N-BOC-L-alanine (Sigma) and L-phenylalanine methyl ester (Sigma) using General Procedure A, followed by removal of the BOC-group using General Procedure Y) and dec-4-enoic acid prepare from ethyl dec-4enoate (ICM) using General Procedure N), the title compound was prepared as a solid (mp =115.5-117.5° C.). The reaction was monitored by tlc (Rf=0.52 in 50% EtOAc/hexanes; 0.60 in 10% CH3OH/CH2Cl2) and the product was purified by flash chromatography using 10% CH3OH/CH2Cl2 as the eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211235B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-1c6752b8c8aa4a28ace8a27e03593a5b |
| Source note | uspto-grants-2001_04 |