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4 protocols using 4 nitrobenzenesulfonylchloride

1

Spectroscopic Characterization of L-Tryptophan Derivative

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Na2CO3 and HCl were obtained from Fluka, while 4-nitrobenzenesulfonylchloride and L- tryptophan were obtained from Sigma-Aldrich. Infrared spectra were recorded on a Bruker FT-IR spectrophotometer. The NMR data were recorded in methanol-d4 on a Bruker DPX-300 spectrometer with 1H at 400 MHz and 13C at 400 MHz. Chemical shifts, δ, are given in ppm and referenced to tetramethylsilane (TMS). The mass spectrum was collected on a Bruker MicrOTOF spectrometer in the positive ion mode using pneumatically assisted electrospray ionization: capillary voltage, 2900 V; sample cone voltage, 15 V; extraction voltage, 1 V; source temperature, 80 °C; desolvation temperature, 160 °C; cone gas flow, 100 Lh−1; desolvation gas flow, 100 L h−1; collision voltage, 2 V; and MCP voltage, 2400 V.
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2

Synthesis and Characterization of Sulfonyl Compounds

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All chemicals were purchased off the analytical grade. 4-bromomethylbenzenesulfonyl chloride, 1,3-diaminopropane, 4-nitrobenzene-sulfonyl chloride, and Et3N from Sigma-Aldrich (USA). All solvents from Tedia (USA). Tris, FeCl3, AlCl3, and K2CO3 from Merck (Germany). Uranyl nitrate from BDH (England) and the uranium nitrate standard solution (1000 μg/mL U in 2%–5% aqueous HNO3) from AccuStandard, (USA).
1H-NMR and 13C-NMR were done on a 400 MHz Bruker instrument using DMSO as a solvent. The infrared spectra were recorded on a Tensor II FT-IR spectrometer with an ATR attachment from Bruker. UV-Vis spectra were recorded using a SPECORD 200 PLUS spectrophotometer, Analytik-Jena (Germany). Elemental analysis was performed using a FLASH 2000 CHNS/O Analyzer, Thermo-Scientific (USA). Thermal gravimetric analysis (TGA) was observed at a rate of 10 °C/min up to 900 °C under N2 in alumina crucibles using a Netzsch TG 209F1 instrument. The sample mass range was 4.74–13.55 mg.
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3

Synthesis and Characterization of Oxazoline Polymers

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Maleic anhydride (99%, Bernd Kraft), furan (99%, Acros), ethanolamine (99%, Acros), 4-toluenesulfonyl chloride (99%, Acros), 4-nitrobenzenesulfonyl chloride (97%, Sigma-Aldrich), pyridine (99%, Roth), tetramethylammonium hydroxide (25 wt% in methanol, Acros), bovine serum albumin (BSA; Sigma), toluene (Fisher), petroleum ether (Acros), ethanol (99.8%, Acros), acetone (Fisher), tetrahydrofuran (THF; VWR), diethyl ether (99.5%, Roth), and dichloromethane (DCM; VWR) were used as received. Acetonitrile (MeCN; Sigma-Aldrich) was dried in a solvent purification system (JC Meyer) before use as a polymerization solvent. 2-Ethyl-2-oxazoline (EtOx; Aldrich) was distilled over barium oxide and stored under argon.
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4

Synthesis and Characterization of Novel Compound

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Na2CO3, NaCl, and 20% HCl were obtained from Fluka, while 4-nitrobenzene sulfonyl chloride and 4-hydroxyproline were obtained from Sigma Aldrich (Bristol Scientific Nigeria). IR spectra were recorded on Bruker FT-IR spectrophotometer. The NMR peaks were recorded on Bruker DPX 300 spectrophotometer with 1H at 400 MHz and 13 ℃ at 100 MHz. Chemical shifts δ are given in ppm and referenced to tetramethylsilane. Methanol was used as a solvent for crystallization. X-ray data of the single crystal were collected on an XtaLAB Synergy, Dualflex, Pilatus 200 K diffractometer using CuKα radiation at 105.4 (7)K. The pharmacokinetic properties were studied using SwissADME free online tool (https://www.swissadme.ch), while the Molecular docking was carried out using the Molecular operating environment (MOE) (AutoDock Vina, BIOVIA).
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