HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889012Generated: October 29, 2026
Dimethyl Sulfoxide → HCID 57988793, compound
https://huagongshe.com/reaction/889012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 57988780 | HCID 57988780 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57988793 | HCID 57988793 | 85% |
Reaction Steps
A mixture of 1,3-dipropyl-8-(1-prop-2-ynyl-1H-pyrazol-4-yl)-7-(2-trimethylsilanyl-ethoxymethyl)-3,7-dihydro-purine-2,6-dione (0.1 g, 0.212 mmol), N-methyl piperazine (0.025 g, 0.254 mmol), formaldehyde (0.08 ml), CuI (0.008 g), and DMSO (2 ml) was stirred at 30° C. for 72 hours. The mixture was cooled to 25° C. and the residue was diluted with water (10 ml) and extracted with ethylacetate (2×10 ml). The organic layer was washed with saturated brine solution (50 ml) and dried over Na2SO4. The solvent was evaporated to obtain pure 8-{1-[4-(4-Methyl-piperazin-1-yl)-but-2-ynyl]-1H-pyrazol-4-yl}-1,3-dipropyl-7-(2-trimethylsilanyl-ethoxymethyl)-3,7-dihydro-purine-2,6-dione (0.105 g, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252797B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-e9a6bd4ca36549a890fb6fba445d4f4c |
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| Source note | uspto-grants-2012_08 |
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