HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 4-(2-{[4-((R)-1-Benzyloxycarbonyl-ethoxy)-7-methyl-quinoline-2-carbonyl]amino}-acetyl)-piperazine-1-carboxylic acid butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | benzyl (2S)-2-hydroxypropanoate | HCID 11052238 | — |
| Reactant | HCID 178452377 | HCID 178452377 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2-{[4-((R)-1-Benzyloxycarbonyl-ethoxy)-7-methyl-quinoline-2-carbonyl]amino}-acetyl)-piperazine-1-carboxylic acid butyl ester | HCID 68601487 | — |
Reaction Steps
To a solution of 6 g 4-{2-[(4-Hydroxy-7-methyl-quinoline-2-carbonyl)-amino]-acetyl}-piperazine-1-carboxylic acid butyl ester and 2.5 g benzyl-L-lactate in 97 ml THF were added 5.5 g triphenylphosphine and 3.6 g diethylazodicarboxylate. After stirring for 16 h at RT LCMS indicated complete conversion and water was added to the reaction mixture which was then extracted with ethyl acetate. The residue obtained after evaporation of the solvent was purified by flash chromatography on silica using an ethyl acetate/heptane gradient. Yield: 5.5 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08669266B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-08dacfcab2e0441fbdb828bec6661bf3 |
| Source note | uspto-grants-2014_03 |