HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl chloroformate → HCID 71486752, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(aminomethyl)-7-chloro-1-phenylquinolin-4(1H)-one | HCID 71208398 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71486752 | HCID 71486752 | — |
Reaction Steps
In a 10 mL round-bottomed flask, 3-(aminomethyl)-7-chloro-1-phenylquinolin-4(1H)-one intermediate D (0.05 g, 0.176 mmol), phenyl chloroformate (27.5 mg, 0.176 mmol) and N,N-diisopropylethylamine (68.1 mg, 92.0 μL, 0.527 mmol) were combined with CH2Cl2 (3 mL). The reaction mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated, then the crude product was purified using preparative reverse-phase HPLC to provide (7-chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-carbamic acid phenyl ester. MS calcd. for C24H18ClN5O [(M+H)+] 405.1, obsd. 404.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501732B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-bf73a01b940c4b45abfec0ff6d8fb367 |
| Source note | uspto-grants-2013_08 |