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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851756Generated: November 2, 2026

Pyridine → N-[2-(6-methoxypyridin-3-yl)-1,3-benzothiazol-6-yl]methanesulfonamide

https://huagongshe.com/reaction/1851756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-(6-Methoxypyridin-3-yl)-1,3-benzothiazol-6-amineHCID 24803565—
CatalystHexaneHCID 8058—
SolventDichloromethaneHCID 6344—
ProductN-[2-(6-methoxypyridin-3-yl)-1,3-benzothiazol-6-yl]methanesulfonamideHCID 2480356770.2%

Reaction Steps

Mesylchloride (3 μL, 0.037 mmol) and pyridine (3 μL, 0.037 mmol) was added to a sol. 2-(6-methoxypyridin-3-yl)-1,3-benzothiazol-6-amine (9 mg, 0.034 mmol) in DCM (1 mL). The r.m. was stirred at r.t. for 6 days. A few drops of hexane was added and the precipitated solid was collected and dried in vacuo. The crude product was purified by flash column chromatography (20 to 100% ethyl acetate in heptane), to give the title compound (8 mg) as an off-white solid. 1H NMR δ 9.84 (s, 1 H) 8.63 (d, 1 H) 8.11 (dd, 1H) 7.77 (d, 1 H) 7.71 (d, 1 H) 7.14 (dd, 1 H) 6.79 (d, 1 H) 3.73 (s, 3 H) 2.82 (s, 3 H); MS m/z (M+H) 336, (M−H) 334.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957215B2
Source datasetuspto-grants-2015_02
ORD IDord-8fd08980f36b4ab3af1a3e1ae7f1c4bb
Source noteuspto-grants-2015_02