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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Quinolinecarboxylic acidHCID 10243—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantFmoc-4-Amino-L-phenylalanineHCID 7019927—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-[(4-quinolinylcarbonyl)amino]-L-phenylalanineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06229011B1
Source datasetuspto-grants-2001_05
ORD IDord-a3e9b73cf2874c33a8560e0a483ef808
Source noteuspto-grants-2001_05