HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 66653126, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Methoxy-2-phenylindolizine | HCID 13400125 | — |
| Reactant | HCID 66653415 | HCID 66653415 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 66653126 | HCID 66653126 | 69.3% |
Reaction Steps
2.25 ml (16.12 mmol) of triethylamine and 3 g (13.44 mmol) of 1-methoxy-2-phenylindolizine (according to the method described in WO 03/084956) diluted in 20 ml of dichloroethane are added, under an inert atmosphere at ambient temperature, to 4.22 g (14.78 mmol) of 4-oxo-2-phenyl-4H-3,1-benzoxazine-6-carboxylic acid (described in WO 06/097625) in 100 ml of dichloroethane. After stirring overnight at ambient temperature, the reaction medium is filtered, and rinsed with dichloroethane. The filtrate is washed with water, dried over sodium sulphate, filtered, and concentrated under reduced pressure. The residue is filtered through a silica pâté, elution being carried out with dichloromethane. 4.4 g of a yellow solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859544B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-2a3bf76650df4f01af2e44ce62e3f122 |
| Source note | uspto-grants-2014_10 |