HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099660Generated: October 26, 2026
N,N-Diethylethylenediamine → (S)-N-[(2-{[2-(diethylamino)ethyl]amino}-2-oxoethyl)(oxo)phenyl-lambda6-sulfanylidene]-5-[(3-hydroxyphenyl)ethynyl]nicotinamide
https://huagongshe.com/reaction/1099660
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Diethylethylenediamine | HCID 60993 | — |
| Reactant | (S)-Ethyl [N-({5-[(3-hydroxyphenyl)ethynyl]pyridin-3-yl}carbonyl)-S-phenylsulfonimidoyl]acetate | HCID 24954917 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-N-[(2-{[2-(diethylamino)ethyl]amino}-2-oxoethyl)(oxo)phenyl-lambda6-sulfanylidene]-5-[(3-hydroxyphenyl)ethynyl]nicotinamide | HCID 24954918 | 60.3% |
Reaction Steps
(S)-Ethyl [N-({5-[(3-hydroxyphenyl)ethynyl]pyridin-3-yl}carbonyl)-S-phenylsulfonimidoyl]acetate (73 mg, 0.16 mmol) in anhydrous MeOH (1.5 mL) was added N,N-diethylethylenediamine (0.12 mL, 0.84 mmol) dropwise. The reaction mixture was heated at 30° C. for 4 hours. The reaction mixture was evaporated and the residue was partitioned between EtOAc and saturated aqueous NaHCO3. The organic layer was washed once with brine, dried (anhydrous Na2SO4), concentrated. The residue was purified by chromatography (silica gel, 50:1 CHCl3:MeOH to 10:1 CHCl3:MeOH). The product containing fractions were concentrated to give the title compound as a foamy solid (50 mg, 59%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143410B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-fd60944e6731406b93467a627a724d3b |
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| Source note | uspto-grants-2012_03 |
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