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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408758Generated: October 27, 2026

Lithium Hydroxide → 1-(4-Bromo-6-fluoro-1H-benzoimidazol-2-yl)-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/408758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantTetrahydrofuranHCID 8028—
Reactant1-(4-Bromo-6-fluoro-1H-benzoimidazol-2-yl)-1H-pyrazole-4-carboxylic acid ethyl esterHCID 66937375—
SolventWaterHCID 962—
Product1-(4-Bromo-6-fluoro-1H-benzoimidazol-2-yl)-1H-pyrazole-4-carboxylic acidHCID 5815608167%

Reaction Conditions

Temperature23 °C

Reaction Steps

A mixture of 1-(4-bromo-6-fluoro-1H-benzoimidazol-2-yl)-1H-pyrazole-4-carboxylic acid ethyl ester (16.0 mg, 45.0 mmol), LiOH (10.0 mg, 0.230 mmol), THF (0.5 mL), and H2O (0.17 mL) was stirred at 23° C. for 16 h. THF was removed under reduced pressure and then aqueous HCl was added. The resulting precipitate was collected and washed with water to yield the titled compound (10.0 mg, 67%). MS (ESI/CI): mass calcd. for C11H6BrFN4O2, 325.1; m/z found, 326.0 [M+H]+. 1H NMR (400 MHz, DMSO-d6): 13.82 (s, 1H), 12.94 (s, 1H), 8.87 (s, 1H), 8.30 (d, J=0.5 Hz, 1H), 7.45 (dd, J=9.6, 2.3 Hz, 1H), 7.32 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759345B2
Source datasetuspto-grants-2014_06
ORD IDord-45c64cd83bc0403c8451344fe5ca97ad
Source noteuspto-grants-2014_06