HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694730Generated: November 1, 2026
Citric Acid → 5-Bromo-4-methyl-2-(5-methyl-1,1-dioxido-1,2,5-thiadiazolidin-2-yl)-pyrimidine
https://huagongshe.com/reaction/1694730
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Methyl-1,2,5-thiadiazolidine 1,1-dioxide | HCID 10393280 | — |
| Reactant | 2,5-Dibromo-4-methylpyrimidine | HCID 66521322 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromo-4-methyl-2-(5-methyl-1,1-dioxido-1,2,5-thiadiazolidin-2-yl)-pyrimidine | HCID 67279826 | — |
Reaction Steps
Sodium hydride (0.128 g, 60% disp. in oil) was added to a stirred solution of 2-methyl-1,2,5-thiadiazolidine 1,1-dioxide (0.433 g) in THF (10 ml). DMF (10 ml) was added and the mixture heated at 80° C. for 5 min then a solution of the product from step (i) (0.8 g) in DMF (5 ml) was added. The mixture was heated at 60° C. for 10 min, poured into water (100 ml), acidified with citric acid and extracted with ethylacetate. The organics were evaporated under reduced pressure and the residue purified by chromatography on silica eluting with diethylether, yield 0.58 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158820B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-724383c940b246ad8351d938555d76a3 |
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| Source note | uspto-grants-2012_04 |
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