Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804086Generated: October 31, 2026

4-Bromo-2-methylaniline → HCID 67380949, compound

https://huagongshe.com/reaction/1804086

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-methylanilineHCID 11423—
ReactantN,N-bis(2-chloroethyl)-p-toluenesulphonamideHCID 96039—
ReactantCyclopropylboronic acidHCID 2760897—
ProductHCID 67380949HCID 6738094935.2%

Reaction Steps

By reaction and treatment in the same manner as in Preparation Example 15 and using 4-bromo-2-methylaniline (3 g), N,N-bis(2-chloroethyl)-4-methylbenzenesulfonamide (5.65 g) and cyclopropylboronic acid (721 mg), 1-(4-cyclopropyl-2-methylphenyl)piperazine (640 mg) was obtained. To a solution (7 mL) of 6-bromonicotinic acid (132 mg) in methanol were added 1-(4-cyclopropyl-2-methylphenyl)piperazine (150 mg) and 4-(4,6-dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (DMT-MM) (217 mg), and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated. The residue was purified by column chromatography (ethyl acetate:hexane) to give the title compound (260 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354401B2
Source datasetuspto-grants-2013_01
ORD IDord-55ff69408e3a46e0a701ee1e91161f0d
Source noteuspto-grants-2013_01