HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-2,3-dichlorobenzene → 1-(2,3-Dichlorophenyl)-[1,4]diazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-2,3-dichlorobenzene | HCID 42066 | — |
| Reactant | [1,4]Diazepine-1-carboxylic acid tert-butylester | HCID 57499755 | — |
| Reactant | (+/-)-2,2-Bis(diphenylphosphino)-1,1-binaphthyl | HCID 86595863 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(2,3-Dichlorophenyl)-[1,4]diazepine | HCID 68631489 | — |
Reaction Steps
2.25 g (10 mmol) 1-bromo-2,3-dichloro-benzene was dissolved in dry toluene (50 ml), 2.3 (11 mmol) of [1,4]diazepine-1-carboxylic acid tert-butylester was added followed by 0.2 g BINAP (2,2-bis(diphenylphosphino)-1,1′-binaphtyl), 85 mg tris(dibenzylideneacetone)dipalladium(0) and 1.2 g (12 mmol) sodium-tert-butoxyde. The reaction mixture was refluxed for eight hours and filtered. The organic layer was washed with water, dried and evaporated in vacuo. The residue was purified by chromatography and deprotected at 10° C. using 20 ml ethylacetate saturated with gaseous hydrochloric acid, the precipitate was filtered giving 2.1 g (yield: 75%) hydrochloride salt of the title compound, melting at 182-3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737142B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-7a73e7e5afb045feb1e989fcb8ce389d |
| Source note | uspto-grants-2010_06 |