HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976962Generated: November 1, 2026
4-Quinolinecarboxylic acid → 4-[(4-quinolinylcarbonyl)amino]-L-phenylalanine
https://huagongshe.com/reaction/1976962
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Quinolinecarboxylic acid | HCID 10243 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | Fmoc-4-Amino-L-phenylalanine | HCID 7019927 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 4-[(4-quinolinylcarbonyl)amino]-L-phenylalanine | HCID 53733986 | — |
Reaction Steps
A 250 mL cylindrical glass vessel equipped with a coarse glass frit was charged with 4-amino-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine on Wang resin (10 g) obtained in Example 36 and a solution prepared from quinoline-4-carboxylic acid (5.2 g, 30 mmol), BOP (13.75 g, 30 mmol) and diisopropylethylamine (6.8 mL) in 70 mL of NMP. The slurry was agitated for 4 hours. The mixture was filtered and washed with dichloromethane (2×100 mL), methanol (2×100 mL) and dimethylformamide (2×100 mL). To the washed resin was added a solution of 25% piperidine in NMP (80 mL), the mixture was agitated at room temperature for 20 minutes and filtered. The process was repeated and the resulting slurry was filtered and washed with dichloromethane (2×100 mL), methanol (2×100 mL) and dimethylformamide (2×100 mL). Filtration afforded 4-[[(4-quinolinyl)carbonyl]amino]-L-phenylalanine on Wang resin suitable for use in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06229011B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-a3e9b73cf2874c33a8560e0a483ef808 |
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| Source note | uspto-grants-2001_05 |
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