HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521676Generated: October 29, 2026
Ethylene Glycol → HCID 118205820, compound
https://huagongshe.com/reaction/521676
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-[2-(2-Ethylsulfanylphenyl)-7-trifluoromethylpyrido[3,2-d]pyrimidin-4-yl]-2-tosylhydrazine | HCID 118034990 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 118205820 | HCID 118205820 | 39.7% |
Reaction Steps
A mixture of 156 mg of 1-[2-(2-ethylsulfanylphenyl)-7-trifluoromethylpyrido[3,2-d]pyrimidin-4-yl]-2-tosylhydrazine and 12 ml of ethylene glycol was added to a mixture of 4 ml of an 8% aqueous sodium hydroxide solution and 2 ml of ethylene glycol at 80° C., and the mixture was stirred at 100° C. for 40 minutes. Water was added to the cooled reaction mixture, and the mixture was extracted with t-butyl methyl ether. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The mixture was concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 40 mg of 2-(2-ethylsulfanylphenyl)-7-trifluoromethylpyrido[3,2-d]pyrimidine (Compound of Present Invention 18).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328121B1 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-d3e94638df1f4ff9a75621307fcb98e4 |
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| Source note | uspto-grants-2016_05 |
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