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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358367Generated: October 27, 2026

2-Thiophenesulfonyl chloride → 5-methyl-N-[6-(2-(2-thiophenesulfonylamino)-ethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-2-pyridine sulfonamide

https://huagongshe.com/reaction/1358367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
Reactant5-methyl-N-[6-(2-aminoethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-2-pyridine sulfonamideHCID 18184254—
Product5-methyl-N-[6-(2-(2-thiophenesulfonylamino)-ethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-2-pyridine sulfonamideHCID 18184179—

Reaction Steps

According to the procedure described in Example 4a) 107 mg 5-methyl-N-[6-(2-aminoethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-2-pyridine sulfonamide was reacted with thiophene-2-sulfonylchloride to give 135 mg 5-methyl-N-[6-(2-(2-thiophenesulfonylamino)-ethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-2-pyridine sulfonamide. LC-MS: tR=4.33 min, [M+1]+=655.46, [M−1]−=653.50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596719B1
Source datasetuspto-grants-2003_07
ORD IDord-27bbd56defd747f8a4bc99ee55be4295
Source noteuspto-grants-2003_07