HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 15895694, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (S)-1-N-Boc-piperidine-2-ethanol | HCID 1514243 | — |
| Reactant | 7-chloro-3-(3,5-dimethylphenyl)-4-hydroxy-6-nitro-1H-quinolin-2-one | HCID 54711238 | — |
| Product | HCID 15895694 | HCID 15895694 | — |
Reaction Steps
To a solution of (S)-2-(2-hydroxyethyl)-piperidine-1-carboxylic acid tert-butyl ester (0.864 g in 38 mL dry tetrahydrofuran) was added 1.56 g of 7-chloro-3-(3,5-dimethylphenyl)-4-hydroxy-6-nitro-1H-quinolin-2-one [see Example 9] followed by 1.19 g of triphenylphosphine and the mixture stirred at room temperature. To this was added 0.72 mL of diethyl azodicarboxylate (DEAD) and stirring was continued for 64 hours. At this time the solvents were removed in vacuo and the residue purified by flash chromatography on silica gel (hexane:ethyl acetate, 6:4) to give the title compound, 1.56 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06147088 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-97bcf282d52f4e4e9a662c112a279649 |
| Source note | uspto-grants-2000_11 |