HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172297Generated: October 26, 2026
Benzaldehyde → 2-(4-Oxo-2-phenyl-3-((pyridin-4-yl)methyl)thiazolidin-5-yl)acetic acid
https://huagongshe.com/reaction/1172297
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | (+-)-Mercaptosuccinic acid | HCID 6268 | — |
| Reactant | 4-Pyridineethanamine | HCID 83275 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Oxo-2-phenyl-3-((pyridin-4-yl)methyl)thiazolidin-5-yl)acetic acid | HCID 59555308 | — |
Reaction Steps
A solution of benzaldehyde (0.75 mmol, 79.6 mg) and 2-(pyridin-4-yl)ethanamine (97.3 mg, 0.9 mmol) in DMF (0.5 ml) with 4 Å molecular sieves was heated at 80° C. for 2 hours. A solution of mercaptosuccinic acid (1.13 mmol, 168 mg) in DMF (0.2 ml) was added and the reaction was heated at 80° C. for an additional 16 hours. The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was washed with 1N HCl, water and evaporated to dryness to give the desired product which was used without further purification. LC/MS (10% to 99%): M/Z (M+H)+ (obs)=329; tR=1.95.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834000B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-e29dbc8f502d4389b971611e3f014ced |
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| Source note | uspto-grants-2010_11 |
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