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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389579Generated: October 30, 2026

Potassium Carbonate → 7-Bromo-6-(3-fluorophenyl)-1,2-benzothiazole

https://huagongshe.com/reaction/389579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant3-Fluorophenylboronic acidHCID 2733986—
Reactant7-Bromo-6-iodo-1,2-benzothiazoleHCID 66760283—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product7-Bromo-6-(3-fluorophenyl)-1,2-benzothiazoleHCID 6676067660.4%

Reaction Steps

A suspension of 7-bromo-6-iodo-1,2-benzothiazole (29.6 mg, 0.0871 mmol), 3-fluorobenzeneboronic acid (12.8 mg, 0.0915 mmol), potassium carbonate (39.2 mg, 0.284 mmol), and Pd(PPh3)4 (12.2 mg, 0.0106 mmol) in 4:1 1,4-dioxane:water (1 mL) was heated to 80° C. for 15 h. The reaction mixture was concentrated in vacuo. Purification of the residue by ISCO chromatography (0 to 100% dichloromethane:heptane) to afford 16.2 mg (59%) of the title compound as a white solid. 1H NMR (400 MHz, CDCl3): δ 9.08 (s, 1H), 7.73 (d, J=7.58 Hz, 1H), 7.52 (dt, J=5.81, 7.96 Hz, 1H), 7.37 (qd, J=0.88, 7.71 Hz, 1H), 7.33 (d, J=7.58 Hz, 1H), 7.28-7.31 (m, 1H), 7.20 (ddt, J=1.01, 2.59, 8.43 Hz, 1H); MS (ESI): 307.87, 309.86 [M+H]+; HPLC tR=4.33 min (ZQ3: nonpolar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378104B2
Source datasetuspto-grants-2013_02
ORD IDord-e81f841c1cb3476a8b8ff578acd890e0
Source noteuspto-grants-2013_02