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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356811Generated: November 2, 2026

Methanol → 4'-[(6-Fluoro-1,3-benzothiazol-2-yl)amino]-3-chlorobiphenyl-4-carboxylic acid

https://huagongshe.com/reaction/2356811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 59385209HCID 59385209—
SolventTetrahydrofuranHCID 8028—
Product4'-[(6-Fluoro-1,3-benzothiazol-2-yl)amino]-3-chlorobiphenyl-4-carboxylic acidHCID 59385271—

Reaction Conditions

Temperature50 °C

Reaction Steps

Methyl 4′-[(6-fluoro-1,3-benzothiazol-2-yl)amino]-3-chlorobiphenyl-4-carboxylate (0.30 g, 0.71 mmol) was suspended in THF (5 mL), MeOH (5 mL) and water (2.5 mL), and then NaOH (0.28 g, 7.1 mmol) was added. The reaction mixture was heated at 50° C. for 3 h. Upon cooling to rt, the reaction mixture was concentrated under reduced pressure, acidified, and the resulting solid was collected by filtration. This yielded 0.34 g (quantitative) of the title compound. LC/MS m/z 399.2 (MH+), retention time 3.53 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759376B2
Source datasetuspto-grants-2010_07
ORD IDord-f70a7edf0e7c47a9b12879a2ab8c0c5c
Source noteuspto-grants-2010_07