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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092782Generated: October 27, 2026

Sodium Thiosulfate → Methyl 6-chloro-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinate

https://huagongshe.com/reaction/2092782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantMethyl 6-chloro-4-cyano-2-(3-(methylthio)phenylamino)nicotinateHCID 58317663—
SolventDimethylformamideHCID 6228—
ProductMethyl 6-chloro-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinateHCID 5831771650%

Reaction Steps

To a solution of methyl 6-chloro-4-cyano-2-(3-(methylthio)phenylamino)nicotinate (291.1 mg, 0.872 mmol) in DMF (10 mL) was added m-chloroperoxybenzoic acid (538.9 mg, 2.405 mmol) at 0° C. The mixture was stirred at RT for 16 h. Aqueous Na2S2O3 (30 mL) was added and the mixture was extracted with EtOAc (2×30 mL). The organic layers were washed with saturated aq NaHCO3 (20 mL), water (20 mL) and brine (20 mL), were dried over anhydrous Na2SO4, and then filtered (DM1020). The filtrate was concentrated under reduced pressure and the residue was washed with IPE to give the title compound as a yellow solid (158.2 mg, 50%). 1H-NMR (CDCl3) δ ppm 3.11 (s, 3H), 4.07 (s, 3H), 7.10 (s, 1H), 7.57-7.60 (m, 1H), 7.70-7.72 (m, 1H), 7.91-7.93 (m, 1H), 8.25-8.26 (m, 1H), 10.73 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440689B2
Source datasetuspto-grants-2013_05
ORD IDord-a27862c86b0a4660ba285e8b6ac827bc
Source noteuspto-grants-2013_05