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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358353Generated: November 3, 2026

N-(3-hydroxypropyl)-4-methylbenzenesulfonamide → 5-isopropyl-N-[6-(3-(4-methylbenzenesulfonylamino)-propoxy)-5-(o-methoxyphenoxy)-2-methyl-4-pyrimidinyl]-2-pyridine sulfonamide

https://huagongshe.com/reaction/1358353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-hydroxypropyl)-4-methylbenzenesulfonamideHCID 2180655—
Reactant5-isopropyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-2-pyridine sulfonamideHCID 22729411—
SolventTetrahydrofuranHCID 8028—
Product5-isopropyl-N-[6-(3-(4-methylbenzenesulfonylamino)-propoxy)-5-(o-methoxyphenoxy)-2-methyl-4-pyrimidinyl]-2-pyridine sulfonamideHCID 18184225—

Reaction Steps

According to the procedure described in Example 1a) 256 mg 5-isopropyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-2-pyridine sulfonamide was reacted with N-(3-hydroxy-propyl)-4-methylbenzenesulfonamide in THF in the presence of potassium tert.-butylate to give 280 mg 5-isopropyl-N-[6-(3-(4-methylbenzenesulfonylamino)-propoxy)-5-(o-methoxyphenoxy)-2-methyl-4-pyrimidinyl]-2-pyridine sulfonamide. LC-MS: tR=4.83 min, [M+1]+=705.70, [M−1]−=703.79.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596719B1
Source datasetuspto-grants-2003_07
ORD IDord-b8a59f9f72fe41ddbe900e5c1375bd38
Source noteuspto-grants-2003_07