HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261090Generated: November 3, 2026
Ethylamine → 5-{[3-(Ethylamino)-4-nitrophenyl]methylidene}-1,3-thiazolidine-2,4-dione
https://huagongshe.com/reaction/2261090
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 5-[(3-Fluoro-4-nitrophenyl)methylidene]-1,3-thiazolidine-2,4-dione | HCID 71378270 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 5-{[3-(Ethylamino)-4-nitrophenyl]methylidene}-1,3-thiazolidine-2,4-dione | HCID 71378269 | — |
Reaction Steps
5-(3-Fluoro-4-nitro-benzylidene)-thiazolidine-2,4-dione (200 mg, 0.75 mmol, 1 eq.), was dissolved in DME (6 mL) and TEA (208 μL, 1.5 mmol, 2 eq.) and a solution of ethylamine (2 eq.) was added. The reaction mixture was shaken at 60° C. over night. The solvent was removed in vacuo and residue dissolved in ethyl acetate and washed with 10% ammonium chloride aqueous solution. The organic layer was dried on Na2SO4 and the solvent evaporated to give the corresponding aniline derivative as either red oil, which was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07846925B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-196f00412982452d81ee7473a9441538 |
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| Source note | uspto-grants-2010_12 |
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