Nitroreductase (NTR) is a flavoenzyme with β-nicotinamide adenine dinucleotide (NADH) or β-nicotinamide adenine dinucleotide phosphate (NADPH) as a cofactor. NTR catalyzes the reduction of nitro compound to correspond in amine. The use of fluorescent probes assists real-time detection of NTR for hypoxia. We prepare a new long-wavelength latent fluorogenic probe, NBF-L, for the monitoring NRT activities. The fluorogenic probes are stable that unmask their intense fluorescence only by a user-designated chemical reaction, and they are especially useful tools for basic research in the biological sciences. The fluorogenic chemical transformation of NBF-L triggered by NRT in the presence of NADH is through a series of tandem reaction which are irreversible in aqueous media. But in the synthesis of latent fluorescent probes NBF-L have some problems and discuss these problems.