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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252731Generated: October 25, 2026

1,2-Dimethoxyethane → n-Propanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amide

https://huagongshe.com/reaction/2252731

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium tert-butoxideHCID 23665647—
Reactantn-Propanesulfonic acid [6-chloro-5-(2-ethoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]amideHCID 86760603—
SolventEthylene GlycolHCID 174—
Productn-Propanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amideHCID 71499649—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of potassium tert.-butoxide (366.5 mg) in ethylene glycol (5 ml) was added 1,2-dimethoxy ethane (5 ml) and n-propanesulfonic acid [6-chloro-5-(2-ethoxy-phenoxy)-[2,2′]bipyrimidinyl-4-yl]amide (420 mg). The reaction mixture was heated to 85° C. for 7 days, concentrated in vacuo, poured onto water, acidified by 2N HCl and extracted with ethyl acetate. The combined organic extracts were dried over magnesium sulfate and concentrated in vacuo. The precipitated product was washed with diethylether, filtered and dried at HV to give n-propanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2′]bipyrimidinyl-4-yl]-amide (401 mg). LC-MS: tR: 3.67, [M+H]+: 462.26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323465B2
Source datasetuspto-grants-2008_01
ORD IDord-fbd0aa49c7214c9e8f99a90e6dec0183
Source noteuspto-grants-2008_01