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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10251Generated: October 25, 2026

Dimethylformamide → 4-i-Propyl-phenyl sulfamic acid-[6-[2-(pyrimidin-2-yloxy)ethoxy]-5-(o-methoxyphenoxy)-2-(4-pyridyl)pyrimidin-4-yl]-amide

https://huagongshe.com/reaction/10251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant2-ChloropyrimidineHCID 74404—
Reactant4-i-Propyl-phenyl sulfamic acid-[6-(2-hydroxy-ethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amideHCID 10302811—
SolventTetrahydrofuranHCID 8028—
Product4-i-Propyl-phenyl sulfamic acid-[6-[2-(pyrimidin-2-yloxy)ethoxy]-5-(o-methoxyphenoxy)-2-(4-pyridyl)pyrimidin-4-yl]-amideHCID 1028276173%

Reaction Conditions

Temperature60 °C

Reaction Steps

4-i-Propyl-phenyl sulfamic acid-[6-(2-hydroxy-ethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide (60 mg, Example 3) was dissolved in THF (8 ml) and sodium hydride (14 mg, 60% dispersion in mineral oil) was added and stirring continued for 10 min. 2-Chloro-pyrimidine (22 mg) was added and the mixture was heated to 60° C. for 90 min. DMF (0.5 ml) was added and the solution was stirred at r.t. for 48 h. The solvents were evaporated, water (12 ml) and a 10/solution of citric acid was added until the pH was 3. The precipitate was filtered off and washed with water and purified by recrystallization from diethyl ether to give 4-i-propyl-phenyl sulfamic acid-[6-[2-(pyrimidin-2-yloxy)-ethoxy]-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide (50 mg). tR=4.80 min, (LC); [M+H]+=630.91 (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094781B2
Source datasetuspto-grants-2006_08
ORD IDord-fd75d1250ff34f74a530d064642bf2d5
Source noteuspto-grants-2006_08