HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198666Generated: October 31, 2026
2-[4-(Aminomethyl)phenyl]benzonitrile → 4'-[(3-butyl-5-oxo-1,5-dihydro-4H-1,2,4-triazol-4-yl)methyl]biphenyl-2-carbonitrile
https://huagongshe.com/reaction/1198666
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-[4-(Aminomethyl)phenyl]benzonitrile | HCID 1393341 | — |
| Reactant | Ethyl valerate carbethoxyhydrazone | HCID 53752329 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4'-[(3-butyl-5-oxo-1,5-dihydro-4H-1,2,4-triazol-4-yl)methyl]biphenyl-2-carbonitrile | HCID 14951052 | — |
Reaction Steps
A mixture of 400 mg (1.923 mmole) of [(2'-cyanobiphenyl-4-yl)methyl]amine, 457 mg (2.12 mmole) of ethyl valerimidate carbethoxyhydrazone (from Example 2, Step A), and 7 mL of ethanol was stirred under N2 in an oil bath at 50° C. for 3 hours and then at 80° C. for 2 days. The mixture was cooled and concentrated. The residue, re-concentrated from toluene, was flash chromatographed over silica gel (gradient elution with 1.5-5% methanol in CH2Cl2) to give the desired product, homogeneous in TLC (90:10 CH2Cl2 --MeOH); mass spectrum (FAB) m/e 333 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05281614 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-c16db8f348be4d7897db20295580dfbb |
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| Source note | uspto-grants-1994_01 |
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