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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977168Generated: November 2, 2026

Benzenesulfonyl chloride → HCID 10501747, compound

https://huagongshe.com/reaction/977168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 10707207HCID 10707207—
ProductHCID 10501747HCID 10501747—

Reaction Steps

Benzene sulphonylchloride (0.94 ml) and 4-amino-7-chloro-3-phenyl-2(1H)-quinolone (1 g) (Example 2) were reacted in a similar manner to that as described in Example 4. An additional step was required to remove the tert butyldimethylsilyl protecting group using methanolic-HCl for 20 mins to afford the title compound (0.050 g); mp 268° C. (ethanol); δ (360 MHz, DMSO-d6) 7.14 (6H, m, aromatics), 7.32 (5H, m, aromatics), 7.49 (1H, m, aromatics), 7.67 (1H, d, J =8.7 Hz, 5H), 10.02 (1H, br s, 4NH), 12.15 (1H, br s, 1NH); m/z 410 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614532
Source datasetuspto-grants-1997_03
ORD IDord-47ffd226103347d88e43f86dc0bd468a
Source noteuspto-grants-1997_03