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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Bromonicotinic acid | HCID 88707 | — |
| Reactant | (S)-(+)-S-Methyl-S-phenylsulfoximine | HCID 25036288 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-5-bromo-N-[methyl(oxido)phenyl--sulfanylidene]nicotinamide | HCID 86629466 | 92.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383825B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-cc230c367bb14ca7bc58f799a4df1643 |
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| Source note | uspto-grants-2013_02 |
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