HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023368Generated: November 1, 2026
Diethyl Pyrocarbonate → HCID 53361738, compound
https://huagongshe.com/reaction/1023368
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Pyrocarbonate | HCID 3051 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 67327057 | HCID 67327057 | — |
| Reactant | HCID 67328153 | HCID 67328153 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53361738 | HCID 53361738 | — |
Reaction Steps
To a solution of (E)-3-{3-chloro-5-methyl-4-[(5-{[4-(trifluoromethyl)benzyl]-oxy}pyridin-2-yl)oxy]phenyl}prop-2-enoic acid (139 mg) and 4-{2-[4-(piperazin-1-ylmethyl)-phenyl]ethoxy}benzonitrile trifluoroacetate (131 mg) in DMF (6 mL) was added DEPC (0.073 mL) and Et3N (0.165 mL) at 0° C. After stirring at 0° C. for 1 hour, to the reaction mixture was added H2O, and extracted with AcOEt. The organic layer was washed with saturated aqueous NaCl, dried over anhydrous MgSO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (AcOEt) to give 4-{2-[4-({4-[(E)-3-{3-chloro-5-methyl-4-[(5-{[4-(trifluoromethyl)benzyl]oxy}pyridin-2-yl)oxy]phenyl}prop-2-enoyl]piperazin-1-yl}methyl)phenyl]ethoxy}benzonitrile as a pale yellow amorphous (195 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722663B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-4be07b9779d742d69c09405ad6250982 |
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| Source note | uspto-grants-2014_05 |
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