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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985167Generated: October 28, 2026

Benzenesulfonyl chloride → HCID 22556005, compound

https://huagongshe.com/reaction/985167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 14627640HCID 14627640—
SolventPyridineHCID 1049—
ProductHCID 22556005HCID 22556005—

Reaction Steps

2-[3-Amino-2-oxo-2H-quinolin-1-yl]acetic acid, (0.206 g, 0.81 mmol) was treated with benzenesulfonyl chloride (0.172 g, 0.97 mmol) in pyridine for one hour. After removing the pyridine, the residue was recrystallized in acetone to yield a white crystal solid as the product, 2-[3-benzenesulfonylamino-2-oxo-2H-quinolin-1-yl]acetic acid, (EX-4A)(0.117 g, y=41%). HPLC-MS (0 to 95% AcCN/6 min @ 1.0 mL/Min @ 254 nm @ 50° C.): retention time 2.85 min, M+H+=359.2 for formula C17H15N2O2S. 1H NMR (400 MHz, Acetone-d6): d 5.12 (s, 2H), 7.28 (t, J=7.2 Hz, 1H), 7.36 (d, J=8.8 Hz, 1H), 7.48-7.63 (m, 4H), 7.75 (dd, J=8, 1.6 Hz, 1H), 7.74 (s, 1H), 8.00-8.03 (m, 2H). 13C NMR (101 MHz, Acetone-d6): d (ppm) 44.8, 115.0, 120.8, 120.9, 123.9, 127.8, 128.1, 129.4, 129.9, 130.1, 134.2, 136.7, 140.4, 158.2, 169.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06870056B1
Source datasetuspto-grants-2005_03
ORD IDord-a0464bc97bfa41558bac916d2320d1d4
Source noteuspto-grants-2005_03