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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691553Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 66908232, compound

https://huagongshe.com/reaction/1691553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantThieno[3,2-b]pyridin-2-ylamine hydrochlorideHCID 66907303—
SolventPyridineHCID 1049—
ProductHCID 66908232HCID 6690823225.2%

Reaction Steps

To a suspension of compound 146-A (0.65 g, 2.91 mmol) in pyridine (30 mL), at rt, was added benzenesulfonyl chloride (0.751 mL, 5.83 mmol), and the reaction was stirred for 16 h. Additional benzenesulfonyl chloride (0.225 mL, 1.76 mmol) was added and the reaction mixture was stirred at rt for an additional 16 h. The solvent was evaporated in vacuo, the residue treated with 1N HCl and extracted several times with dichloromethane and ethyl acetate. The aqueous layer was filtered, dissolved in methanol, and the combined organic extracts were evaporated in vacuo. The resultant residue was purified by reverse phase HPLC, eluting with an MeCN—H2O gradient to afford compound 146-B as an orange solid (0.24 g, 20%). 1H-NMR (CD3CN): δ 6.92 (s, 1H), 7.2 8.0 (d of d, 1H), 7.46 (m, 2H), 7.56 (m, 1H), 7.85 (m, 2H), 8.27 (d, 1H), 8.35 (d, 1H); MS: m/z 291.09 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153682B2
Source datasetuspto-grants-2012_04
ORD IDord-b0e86f9535dd494babb110b56c6d557d
Source noteuspto-grants-2012_04