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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422201Generated: October 25, 2026

4,6-Dichloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidine → 5-Isopropyl-pyridine-2-sulfonic acid 6-chloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-yl-amide

https://huagongshe.com/reaction/1422201

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dichloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidineHCID 21979531—
Reactant5-Isopropyl pyridine-2-sulfonamide potassium saltHCID 131720944—
Product5-Isopropyl-pyridine-2-sulfonic acid 6-chloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-yl-amideHCID 22729406—

Reaction Steps

4,6-Dichloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidine is treated with 5-isopropyl-pyridine-2-sulfonamide potassium salt to form 5-isopropyl-pyridine-2-sulfonic acid 6-chloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-yl-amide. This compound is then added to a solution of sodium in ethylene glycol. After heating, 5-isopropyl-pyridine-2-sulfonic acid 6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-yl-amide is obtained and then added to a solution of pyridine-2-carbonyl azide in dioxane to form pyridin-2-yl-carbamic acid 2-[6-(5-isopropyl-pyridine-2-sulfonylamino)-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-yloxy]-ethyl ester (see EP 0713875A1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080866
Source datasetuspto-grants-2000_06
ORD IDord-aabbd61a1234476d9200efba702ff8a3
Source noteuspto-grants-2000_06