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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57156Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 66906833, compound

https://huagongshe.com/reaction/57156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 66906974HCID 66906974—
SolventPyridineHCID 1049—
ProductHCID 66906833HCID 6690683336%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of compound 145-H (0.46 g, 1.52 mmol) in pyridine (4.6 mL), cooled to 0° C., was added benzenesulfonyl chloride (0.206 mL, 1.60 mmol), and the reaction was heated to 50° C. for 72 h. Additional benzenesulfonyl chloride (0.412 mL, 3.20 mmol) was added and the reaction mixture was heated at 50° C. for an additional 16 h. The solvent was evaporated in vacuo, the residue dissolved in dichloromethane and washed with aqueous sodium bicarbonate. The aqueous layer was acidified with 1N HCl, extracted with dichloromethane, and the organic layer was evaporated in vacuo to afford a yellow solid (0.22 g, 36%) as a 1/3.5 mixture of the 3-bromo- and 3-chloro-substituted compounds, 145-Ia and 145-Ib, respectively. 1H-NMR (DMSO-d6): δ 7.1-7.2 (m, 1H), 7.4-7.6 (m, 3H), 7.8 (m, 2H), 8.1-8.2 (m, 1H), 8.25-8.35 (m, 1H); MS: m/z 465 and 509 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434711B2
Source datasetuspto-grants-2016_09
ORD IDord-83ab5dd2ade24808a966aa1072efd52c
Source noteuspto-grants-2016_09