HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612127Generated: November 1, 2026
Sodium Chloride → N-[4-(3-bromoanilino)-3-cyano-7-methoxyquinolin-6-yl]-4-(dimethylamino)but-2-enamide
https://huagongshe.com/reaction/612127
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Amino-4-[(3-bromophenyl)amino]-7-methoxy-quinoline-3-carbonitrile | HCID 9820645 | — |
| Reactant | (E)-4-Bromo-2-butenoyl Chloride | HCID 11263885 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[4-(3-bromoanilino)-3-cyano-7-methoxyquinolin-6-yl]-4-(dimethylamino)but-2-enamide | HCID 54314768 | 57.1% |
Reaction Steps
To a mixture of 1.9 g (5.1 mmol) of 4-[(3-bromophenyl)amino]-7-methoxy-6-amino-3-quinolinecarbonitrile and 5.3 ml (31 mmol) of Hunig's base in 110 ml of dry THF at 0° C., with stirring, was added a THF solution containing 5.7 g (31 mmol) of 4-bromo crotonyl chloride dropwise. The mixture was stirred for additional 0.5 hour after addition. 100 ml of saturated sodium chloride solution was added to the reaction mixture, then it was extracted with ethyl acetate. The ethyl acetate solution was dried over sodium sulfate and then was added to 40 ml of dimethyl amine solution (2.0 M in THF) at 0° C. dropwise. The solution was stirred an additional 0.5 hour. The mixture was poured into diluted sodium bicarbonate solution. The organic layer was separated and dried over sodium sulfate. Chromatography gave 1.4 g of beige solid: mass spectrum (electrospray, m/e): M+H 480.0 and 481.9.
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-df7626bbc75d466faccfcdce322d4df6 |
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| Source note | uspto-grants-1999_12 |
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