HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 131731169, compound → cyclo-L-Lys(Boc)-L-Glu(OH)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 131731169 | HCID 131731169 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Product | cyclo-L-Lys(Boc)-L-Glu(OH) | HCID 131731170 | — |
Reaction Steps
Cyclo-L-Lys(Boc)-L-Glu(OBzl) (22.2 g, 0.05 mol) was dissolved in 200 ml of trifluorethanol and 1.5 g of palladium black was added. Hydrogen was bubbled through the suspension with stirring for 48 hours. The reaction was monitored by TLC. After the reaction was complete, the catalyst was filtered off and the solvent was evaporated in vacuum. The residual peptide was dissolved in 200 ml of distilled water and the impurities were extracted with 3×100 ml of EtOAc. The water phase was combined and evaporated in vacuum. The precipitate was washed with ether and hexane and dried in air. The yield was 16.7 g (90%). Rf=0.4 (CHCl3:EtOAc:MeOH:32% AcOH=6:3:1:0.1); HPLC data: retention time 12.7 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637521B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-03ffb4e598ee417da158239bee92e0e3 |
| Source note | uspto-grants-2014_01 |