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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282607Generated: October 29, 2026

4-Quinolinecarboxylic acid → 4-[(4-quinolinylcarbonyl)amino]-L-phenylalanine

https://huagongshe.com/reaction/1282607

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 (10 g) obtained in Example 62 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 N-methylpyrrolidinone. The slurry was agitated for 4 hr. 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 N-methylpyrrolidinone (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-quinolinylcarbonyl)amino]-L-phenylalanine on Wang resin suitable for use in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455550B1
Source datasetuspto-grants-2002_09
ORD IDord-c524403393c3485a970fc97faf554bcb
Source noteuspto-grants-2002_09