HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934984Generated: November 1, 2026
4-Methylmorpholine → N-{3-Cyano-4-[(3-methylphenyl)amino]-6-quinolinyl}-2-butynamide
https://huagongshe.com/reaction/1934984
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 2-Butynoic acid | HCID 68535 | — |
| Reactant | 6-Amino-4-[(3-methylphenyl)amino]-3-quinolinecarbonitrile | HCID 22466644 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-{3-Cyano-4-[(3-methylphenyl)amino]-6-quinolinyl}-2-butynamide | HCID 22466592 | 41.5% |
Reaction Steps
Dissolved 597 mg (7.10 mmol) 2-butynoic acid in 25 ml THF under N2 and chilled to 0° C. Added 950 μl (7.30 mmol) isobutyl chloroformate and 780 μl (7.10 mmol) N-methylmorpholine and stirred for 10 minutes. Added dropwise a solution of 778 mg (2.84 mmol 6-amino-4-[(3-methylphenyl)amino]-3-quinolinecarbonitrile, stirred for 15 minutes at 0° C. and then at 25° C. overnight. Stripped solvent and slurried residue with water, drying the gummy solid in vacuo briefly. Boiled solid in ethyl acetate and collected. Recrystallized from DMF, using ethanol to crash out the product, and dried in vacuo, giving 401 mg of yellow-brown solid: mass spectrum (electrospray m/e): M+H=341.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06384051B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-6b606a50aada4af1944e18659b1d1d21 |
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| Source note | uspto-grants-2002_05 |
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