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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874730Generated: November 1, 2026

5-Methylthiophene-2-sulfonyl chloride → 4-[(4-(Methyloxy)-3-{[(5-methyl-2-thienyl)sulfonyl]amino}-1H-indazol-1-yl)methyl]benzamide

https://huagongshe.com/reaction/1874730

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methylthiophene-2-sulfonyl chlorideHCID 12400112—
ReactantHCID 58054524HCID 58054524—
SolventPyridineHCID 1049—
Product4-[(4-(Methyloxy)-3-{[(5-methyl-2-thienyl)sulfonyl]amino}-1H-indazol-1-yl)methyl]benzamideHCID 5945604614%

Reaction Steps

A solution of 4-{[3-amino-4-(methyloxy)-1H-indazol-1-yl]methyl}benzamide (32.4 mg, 0.2 mmol) in pyridine 3.6 mL) was added to 5-methyl-thiophenesulfonyl chloride (for a preparation see Intermediate 32) (0.30 mmol). The reaction mixture was shaken briefly and allowed to stand for 3 h at 21° C. prior to concentration by blowdown. The residue was dissolved in 1:1 MeOH-DMSO (0.6 mL) and purified by Mass Directed AutoPrep on Xbridge column using Acetonitrile Water with an ammonium carbonate modifier (Method C). The solvent was evaporated in vacuo using the Genevac to give the title compound (12.5 mg, 14%). LCMS (System A) RT=0.86 min, ES+ve m/z 457 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304446B2
Source datasetuspto-grants-2012_11
ORD IDord-5734baba6b1b494ab4ad9c777bf10230
Source noteuspto-grants-2012_11