HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062824Generated: November 1, 2026
N,N-Diethylaniline → 4'-{1-[4-(1,4-Dioxaspiro[4.5]dec-8-yl)-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]ethyl}biphenyl-2-carbonitrile
https://huagongshe.com/reaction/2062824
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Diethylaniline | HCID 7061 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Ethyl 2-[1-(2'-cyanobiphenyl-4-yl)ethyl]-3-oxohexanoate | HCID 67009459 | — |
| Reactant | N-(1,4-dioxaspiro[4.5]dec-8-yl)-4H-1,2,4-triazol-3-amine | HCID 178420920 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 4'-{1-[4-(1,4-Dioxaspiro[4.5]dec-8-yl)-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]ethyl}biphenyl-2-carbonitrile | HCID 67009699 | 43% |
Reaction Steps
A mixture of ethyl 2-[1-(2′-cyanobiphenyl-4-yl)ethyl]-3-oxohexanoate (4.80 g), N-(1,4-dioxaspiro[4.5]dec-8-yl)-4H-1,2,4-triazol-3-amine (1.50 g), 1,8-diazabicyclo[5.4.0]undec-7-ene (0.2 mL) and N,N-diethylaniline (20 mL) was stirred at 180° C. overnight, allowed to cool and poured into 1 M hydrochloric acid (100 mL), and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound as a pale-yellow oil (1.50 g, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283353B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-c6a7dff8a1ab4f83b187736491a79825 |
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| Source note | uspto-grants-2012_10 |
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