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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | n-Propanesulfonic acid [6-chloro-5-(2-ethoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]amide | HCID 86760603 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | n-Propanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amide | HCID 71499649 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07323465B2 |
|---|
| Source dataset | uspto-grants-2008_01 |
|---|
| ORD ID | ord-fbd0aa49c7214c9e8f99a90e6dec0183 |
|---|
| Source note | uspto-grants-2008_01 |
|---|