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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516014Generated: October 26, 2026

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

https://huagongshe.com/reaction/516014

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 numberUS09108970B2
Source datasetuspto-grants-2015_08
ORD IDord-cc10d71279734e6fba74b5a996c6620f
Source noteuspto-grants-2015_08