HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934995Generated: October 31, 2026
4-Methylmorpholine → N-{4-[(3-Chloro-4-fluoro-phenyl)amino]-3-cyano-6-quinolinyl}-2-butynamide
https://huagongshe.com/reaction/1934995
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 2-Butynoic acid | HCID 68535 | — |
| Reactant | 6-Amino-4-[(3-chloro-4-fluorophenyl)amino]-3-quinolinecarbonitrile | HCID 11012433 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-{4-[(3-Chloro-4-fluoro-phenyl)amino]-3-cyano-6-quinolinyl}-2-butynamide | HCID 22466664 | 24.4% |
Reaction Steps
Dissolved 336 mg (4.00 mmol) 2-butynoic acid in 20 ml of THF and chilled to 0° C. under N2. Added 520 μl (4.00 mmol) isobutyl chloroformate and 440 μl (4.00 mmol) N-methylmorpholine and stirred for 10 minutes. Added a solution of 500 mg (1.60 mmol) 6-amino-4-[(3-chloro-4-fluorophenyl)amino]-3-quinolinecarbonitrile, stirred for 15 minutes at 0° C. and then at 25° C. overnight. Stripped solvent, washed with water, collected and dried in vacuo. Recrystallized from ethyl acetate, giving 148 mg of a yellow solid: mass spectrum (electrospray m/e): M+H=379.1, 381.1.
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-294c707366b34951a320a5606822467a |
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| Source note | uspto-grants-2002_05 |
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