HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735180Generated: October 26, 2026
Ethanol, 2-(cyclohexylamino)- → (E)-N-(4'-chlorobiphenyl-4-yl)-3-(4-{[cyclohexyl-(2-hydroxyethyl)amino]methyl}phenyl)acrylamide
https://huagongshe.com/reaction/735180
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol, 2-(cyclohexylamino)- | HCID 17827 | — |
| Reactant | (E)-N-(4'-chlorobiphenyl-4-yl)-3-(4-chloromethylphenyl)acrylamide | HCID 68816418 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-N-(4'-chlorobiphenyl-4-yl)-3-(4-{[cyclohexyl-(2-hydroxyethyl)amino]methyl}phenyl)acrylamide | HCID 57845786 | — |
Reaction Steps
0.24 g (1.7 mmol) of 2-cyclohexylaminoethanol are added to a suspension of 130 mg (0.34 mmol) of (E)-N-(4′-chlorobiphenyl-4-yl)-3-(4-chloromethylphenyl)acrylamide in 10 mL of DMF and the mixture is stirred for 48 hours at 80° C. Then the reaction mixture is poured onto water and the precipitate formed is suction filtered and washed with water. The solid is dried in the circulating air dryer at 50° C. Yield: 20 mg (10% of theory); C30H33ClN2O2 (M=489.05); melting point: 178° C.-179° C.; calc.: molecular ion peak (M+H)+: 489/491 (Cl); found: molecular ion peak (M+H)+: 489/491 (Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592373B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-835557360fcd43bf91259c895398a2d1 |
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| Source note | uspto-grants-2009_09 |
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