HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882166Generated: November 1, 2026
Sodium Carbonate → HCID 89630028, compound
https://huagongshe.com/reaction/882166
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3,6-Dihydro-2H-pyran-4-boronic acid pinacol ester | HCID 11218053 | — |
| Reactant | HCID 89630012 | HCID 89630012 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol toluene water | HCID 86587398 | — |
| Product | HCID 89630028 | HCID 89630028 | — |
Reaction Steps
To a solution of 5-bromo-4-(3-nitrophenyl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine (1.00 g, 2.23 mmol) in toluene/EtOH/H2O (4:2:1, 14 mL), was added 2-(3,6-dihydro-2H-pyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.70 g, 3.3 mmol), sodium carbonate (0.70 g, 6.7 mmol) and Pd(PPh3)4 (0.13 g, 0.11 mmol). The resulting solution was stirred for 12 hours at 80° C., cooled, and quenched by the addition of water (50 mL). The resulting solution was extracted with ethyl acetate (×3) and the organic layers were combined, washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The reaction was then purified by chromatography using silica gel, eluting with 1-50% EtOAc/petroleum ether. The product was collected and concentrated in vacuo to afford 5-(3,6-dihydro-2H-pyran-4-yl)-4-(3-nitrophenyl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine as a yellow solid. LRMS (ESI) calc'd for C23H29N4O4Si [M+H]+: 453, found 453.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993756B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-cffb70b2d82d4131a32d8f3234ef9333 |
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| Source note | uspto-grants-2015_03 |
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