HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 67212702, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-(2,4-Dichloro-phenyl)-2,6-dimethyl-pyrazolo[5,1-b]oxazole | HCID 59186007 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67212702 | HCID 67212702 | — |
Reaction Steps
To a solution of 3-(2,4-dichloro-phenyl)-2,6-dimethyl-pyrazolo[5,1-b]oxazole (Intermediate HE) (0.755 g, 2.69 mmol) in DMF (10 ml) is added NBS (0.502 g, 2.82 mmol). The reaction is stirred at RT for 30 mins and then partitioned between Na2CO3 and EtOAc. The mixture is extracted with EtOAc (×2) and the combined organic phases are dried over Na2SO4, filtered and evaporated to dryness under reduced pressure. This resulting solid is recrystallised from hot EtOAc/iso-hexane to yield the title compound. MS: m/z 360.99 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07994203B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-afff5bd28cc7413784a6fd549866e190 |
| Source note | uspto-grants-2011_08 |