HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9728Generated: October 28, 2026
Pyridine → 3-(2-bromo-phenyl)-3,4-dihydro-7-[2-(p-toluenesulfonyl)oxymethyl-benzodioxane-6 yl]amino-1-methyl-pyrimido[4,5-d]pyrimidin-2 (1H)-one
https://huagongshe.com/reaction/9728
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | PharmaGSID_48519 | HCID 10345790 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(2-bromo-phenyl)-3,4-dihydro-7-[2-(p-toluenesulfonyl)oxymethyl-benzodioxane-6 yl]amino-1-methyl-pyrimido[4,5-d]pyrimidin-2 (1H)-one | HCID 86592159 | 26.4% |
Reaction Steps
520 mg of the product from example 1 were dissolved in 20 ml CHCl3. 213 mg tosyl chloride and 13 mg 4-dimethylaminopyridine were added and the mixture was cooled to 5° C. 166 mg pyridine were added dropwise and stirring was continued at room temperature for 3 hrs. The mixture was stirred 1 hr at 60° C., then another 105 mg tosyl chloride were added and stirring was continued at room temperature for 16 hrs. The mixture was diluted with 50 ml CHCl3 and washed with 0.5 M HCl, dried and evaporated. Chromatography on silica yielded 180 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091345B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-2f4ba6433b594125bf21b306ef755b52 |
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| Source note | uspto-grants-2006_08 |
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