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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606610Generated: October 25, 2026

Hydrochloric Acid → 4-[2-(Cyclopropyl-methyl-amino)-thiazol-4-yl]-benzoic acid

https://huagongshe.com/reaction/606610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-[2-(Cyclopropylamino)-1,3-thiazol-4-yl]benzoic acidHCID 59807336—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product4-[2-(Cyclopropyl-methyl-amino)-thiazol-4-yl]-benzoic acidHCID 58256989—

Reaction Steps

4-(2-Cyclopropylamino-thiazol-4-yl)benzoic acid (1.98 mmol), methyliodide (4.36 mmol) and potassium carbonate were mixed in DMF (20 mL) and stirred for 72 hours at room temperature. The mixture was concentrated to dryness and partitioned between dichloromethane and water. The organic layer was dried (MgSO4) and concentrated to dryness. This solid was mixed with THF (4 mL), methanol (2 mL) and 1N LiOH (3 mmol) and heated to 50° C. for 1 hour. The mixture was then cooled to room temperature and 1N HCl was added until pH 4. The mixture was concentrated in vacuo, then the obtained residue was redissolved in dichloromethane-methanol and concentrated onto silica. Flash chromatography of the residue (silica gel, dichloromethane-methanol) gave the title compound as an off-white solid (0.1 g), m/z=275.0 in MS ES+, which was characterised by hplc and MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915300B2
Source datasetuspto-grants-2011_03
ORD IDord-0dd8a922a81f4b33a48f7af3125d1bd1
Source noteuspto-grants-2011_03