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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948432Generated: October 30, 2026

HCID 86623152, compound → HCID 11998796, compound

https://huagongshe.com/reaction/1948432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86623152HCID 86623152—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11998796HCID 1199879687%

Reaction Conditions

Temperature-70 °C

Reaction Steps

N-(5-{2-Bromo-5-[(2-dimethylamino-ethyl)-methyl-sulfamoyl]-thiophen-3-yl}-4-methyl-thiazol-2-yl)-acetamide obtained in Step I as described above (750 mg; 1.56 mmol; 1 eq), is dissolved in anhydrous THF (60 ml). The reaction mixture is cooled down to −70° C. and put under nitrogen. n-Butyllithium (6.2 ml; 1.6 M; 12.5 mmol; 8 eq) is added dropwise. The reaction is stirred 1 hour and is quenched with water. Solvents are evaporated and the resulting residue is dissolved in EtOAc, washed with water (2 times), brine and dried over MgSO4. After evaporation of the solvent, the resulting product is suspended in a mixture of ether-DCM and filtered, affording Compound (36) as a brown solid (582 mg; 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399497B2
Source datasetuspto-grants-2013_03
ORD IDord-1d9fe42154cb4aedb0c6dff751c27197
Source noteuspto-grants-2013_03