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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808648Generated: October 31, 2026

5-Methylthiophene-2-sulfonyl chloride → N-[1-{[3-Fluoro-4-(methyloxy)phenyl]methyl}-4-(methyloxy)-1H-indazol-3-yl]-5-methyl-2-thiophenesulfonamide

https://huagongshe.com/reaction/1808648

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methylthiophene-2-sulfonyl chlorideHCID 12400112—
Reactant1-{[3-Fluoro-4-(methyloxy)phenyl]methyl}-4-(methyloxy)-1H-indazol-3-amineHCID 58054511—
SolventPyridineHCID 1049—
ProductN-[1-{[3-Fluoro-4-(methyloxy)phenyl]methyl}-4-(methyloxy)-1H-indazol-3-yl]-5-methyl-2-thiophenesulfonamideHCID 59456007—

Reaction Steps

A solution of 1-{[3-fluoro-4-(methyloxy)phenyl]methyl}-4-(methyloxy)-1H-indazol-3-amine (for a preparation see Intermediate 80) (130 mg, 0.8 mmol) in pyridine (2 mL) was added to 5-methyl-2-thiophenesulfonyl chloride (0.24 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 (1 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 to give the title compound (76 mg) LCMS (System A) RT=1.11 min, ES+ve m/z 462 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357716B2
Source datasetuspto-grants-2013_01
ORD IDord-65dc35be560746a2aab25488b9f1b9dc
Source noteuspto-grants-2013_01