HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 86649005, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 66994124 | HCID 66994124 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86649005 | HCID 86649005 | 74% |
Reaction Steps
A mixture of tert-butyl 3-[methyl(1-methylethyl)amino]-6,7-dihydropyrazino[2,3-f][1,4]oxazepine-8(9H)-carboxylate (1.0 g), N-bromosuccinimide (608 mg) and acetonitrile (20 mL) was stirred at room temperature for 16 hr. Water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient: 3→30% ethyl acetate/hexane) to give the title compound (915 mg, 74%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318722B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-1eb796da578b4eaba35857ed31cb4e9c |
| Source note | uspto-grants-2012_11 |