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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57158Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 66908232, compound

https://huagongshe.com/reaction/57158

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 numberUS09434711B2
Source datasetuspto-grants-2016_09
ORD IDord-8b5233d2c48c40f2b90229c4a4fffe68
Source noteuspto-grants-2016_09