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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356803Generated: October 25, 2026

Methyl 4-bromobenzoate → Methyl 4'-[(6-fluoro-1,3-benzothiazol-2-yl)amino]biphenyl-4-carboxylate

https://huagongshe.com/reaction/2356803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-bromobenzoateHCID 12081—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
ReactantN-(4-bromophenyl)-6-fluoro-1,3-benzothiazol-2-amineHCID 7147099—
Catalystpalladium(II) acetateHCID 167845—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4'-[(6-fluoro-1,3-benzothiazol-2-yl)amino]biphenyl-4-carboxylateHCID 5827060718%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of bis(pinacolato)diboron (0.35 g, 1.4 mmol), methyl 4-bromobenzoate (0.30 g, 1.4 mmol), palladium(II) acetate (0.01 g, 0.04 mmol), and KOAc (0.41 g, 4.2 mmol) in DMF (7.5 mL) was degassed with argon for 30 min at rt. The mixture was then heated at 80° C. for 4 h. After the mixture was cooled to rt, N-(4-bromophenyl)-6-fluoro-1,3-benzothiazol-2-amine (0.45 g, 1.4 mmol), tetrakis(triphenylphosphine)palladium(0) (0.05 g, 0.04 mmol), and saturated aqueous NaHCO3 (5 mL) were added. The mixture was heated at 85° C. overnight. Upon cooling to rt, the mixture was diluted with EtOAc. The combined organic phases were separated, dried over Na2SO4, and concentrated in vacuo. Purification by column chromatography (25% EtOAc in hexanes) yielded 0.094 g (18%) of the title compound. LC/MS m/z 379.3 (MH+); retention time 3.87 min. 1H NMR (400 MHz, CD3OD) δ 3.93 (s, 3H), 7.05 (t, 1H), 7.39-7.81 (m, 8H), 8.03 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759376B2
Source datasetuspto-grants-2010_07
ORD IDord-ebf7fe45967a444081f0e5a120c008e1
Source noteuspto-grants-2010_07