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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391512Generated: October 25, 2026

Diisopropylethylamine → (S)-5-bromo-N-[methyl(oxido)phenyl--sulfanylidene]nicotinamide

https://huagongshe.com/reaction/391512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromonicotinic acidHCID 88707—
Reactant(S)-(+)-S-Methyl-S-phenylsulfoximineHCID 25036288—
SolventDimethylformamideHCID 6228—
Product(S)-5-bromo-N-[methyl(oxido)phenyl--sulfanylidene]nicotinamideHCID 8662946692.4%

Reaction Steps

To a solution of 5-bromonicotinic acid (1.21 g, 6.0 mmol), N,N-diisopropylethylamine (2.1 mL, 12.0 mmol), and (S)-(+)-S-methyl-S-phenylsulfoximine (931 mg, 6.0 mmol) in DMF (11.0 mL) cooled to 0° C. was treated with 1-benzotriazolyloxytripyrrolidinylphosphonium hexafluorophosphate (PyBOP) (3.43 g, 6.6 mmol). The reaction mixture was stirred 10 minutes, the ice bath removed, and the reaction continued at room temperature for 2 hours. The mixture was taken up in EtOAc and washed with H2O, Na2CO3 solution, brine, AcOH solution, H2O, Na2CO3 solution, brine, dried with anhydrous Na2SO4 and concentrated. The residual brown oil was purified by chromatography (silica gel, hexane/EtOAc). The product containing eluent was concentrated and then triturated with hexane to give the title compound as an off-white solid (1.88 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383825B2
Source datasetuspto-grants-2013_02
ORD IDord-cc230c367bb14ca7bc58f799a4df1643
Source noteuspto-grants-2013_02