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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356650Generated: October 30, 2026

Nitrogen → Pyridin-2-yl-carbamic acid 2-[5-(2-chloro-5-methoxy-phenoxy)-6-(5-isopropyl-pyridin-2-ylsulphonylamino)-pyrimidin-4-yloxy]-ethyl ester

https://huagongshe.com/reaction/356650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant1,4-DioxaneHCID 31275—
ReactantPyridine-2-carbonyl azideHCID 5110493—
ReactantN-[5-(2-chloro-5-methoxy-phenoxy)-6-(2-hydroxy-ethoxy)-pyrimidin-4-yl]-5-isopropyl-pyridine-2-sulphonamideHCID 18938932—
ProductPyridin-2-yl-carbamic acid 2-[5-(2-chloro-5-methoxy-phenoxy)-6-(5-isopropyl-pyridin-2-ylsulphonylamino)-pyrimidin-4-yloxy]-ethyl esterHCID 86753333—

Reaction Conditions

Temperature95 °C

Reaction Steps

100 mg of N-[5-(2-chloro-5-methoxy-phenoxy)-6-(2-hydroxy-ethoxy)-pyrimidin-4-yl]-5-isopropyl-pyridine-2-sulphonamide and 38.5 mg of 2-pyridyl-carboxylic acid azide were dissolved in 1 ml of dry dioxan. The solution was stirred at 95° C. for 2 hours, whereby N2 was liberated. After distillation of the solvent the compound was crystallized from ethanol. 115 mg of pyridin-2-yl-carbamic acid 2-[5-(2-chloro-5-methoxy-phenoxy)-6-(5-isopropyl-pyridin-2-ylsulphonylamino)-pyrimidin-4-yloxy]-ethyl ester were obtained as white crystals with m.p. 190°-191° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05837708
Source datasetuspto-grants-1998_11
ORD IDord-7fa4fae288274be49a4a6fa9a5439110
Source noteuspto-grants-1998_11