HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556437Generated: October 30, 2026
Thiazolidinedione → HCID 11530238, compound
https://huagongshe.com/reaction/556437
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 11630104 | HCID 11630104 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11530238 | HCID 11530238 | 48.8% |
Reaction Steps
A mixture of 2,4-thiazolidinedione (3.4 g; 29.1 mmol; 1.80 eq.), pyrrolidine (269.80 μL; 3.2 mmol; 0.2 eq.) in MeOH (50 mL) was heated at 70° C. A solution of 4-(1-piperidinyl)pyrido[3,2-d]pyrimidine-6-carbaldehyde (Intermediate 1.7) (3.9 g; 16.2 mmol; 1 eq.) in MeOH (50 mL) was slowly added over 1.5 hour at 70° C. After 2 h under reflux after the addition, the reaction was complete. A precipitate was formed. The hot reaction mixture was filtered and the solid was washed with cold MeOH to give (5Z)-5-{[4-(1-piperidinyl)pyrido[3,2-d]pyrimidin-6-yl]methylene}-1,3-thiazolidine-2,4-dione (1) (2.70 g; 48%) as an orange powder in 98% HPLC purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08058289B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-ed5c73411f904ed59d7f6d000c867ad6 |
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| Source note | uspto-grants-2011_11 |
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