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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16119Generated: October 26, 2026

1-Bromo-2,3-dichlorobenzene → 1-(2,3-Dichlorophenyl)-[1,4]diazepine

https://huagongshe.com/reaction/16119

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2,3-dichlorobenzeneHCID 42066—
Reactant[1,4]Diazepine-1-carboxylic acid tert-butylesterHCID 57499755—
Reactant(+/-)-2,2-Bis(diphenylphosphino)-1,1-binaphthylHCID 86595863—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product1-(2,3-Dichlorophenyl)-[1,4]diazepineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737142B2
Source datasetuspto-grants-2010_06
ORD IDord-7a73e7e5afb045feb1e989fcb8ce389d
Source noteuspto-grants-2010_06