HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612016Generated: October 26, 2026
Triethylamine → N-[3-cyano-4-(3,4-dibromophenylamino)quinolin-6-yl]acrylamide
https://huagongshe.com/reaction/612016
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | 6-Amino-4-(3,4-dibromophenylamino)quinoline-3-carbonitrile | HCID 10158966 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-cyano-4-(3,4-dibromophenylamino)quinolin-6-yl]acrylamide | HCID 10116207 | 72.1% |
Reaction Steps
To a solution of 0.75 g (1.79 mmol) of 6-amino-4-[(3,4-dibromophenyl)amino]-3-quinolinecarbonitrile and 0.22 g (2.15 mmol) of triethylamine in 10 mL of tetrahydrofuran was added dropwise 0.195 g (2.15 mmol) of acryloyl chloride. After stirring overnight at 25° C., volatile material was removed and the residue was slurried in water and solid was collected. The crude product was washed with boiling ethyl acetate dried in vacuo (50° C.) to give 0.609 g of brown solid: high resolution mass spectrum (m/e): 470.9457.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06002008 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-da21e736817140b29b3e45a247f02db3 |
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| Source note | uspto-grants-1999_12 |
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