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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984132Generated: October 31, 2026

Benzenesulfonyl chloride → HCID 22556005, compound

https://huagongshe.com/reaction/984132

Reaction equation

Participants

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

Reaction Steps

EX-4A) 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)(0.1 17 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 numberUS06867217B1
Source datasetuspto-grants-2005_03
ORD IDord-6c059d875386468e8cddd8ebacfa858c
Source noteuspto-grants-2005_03