HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858539Generated: October 29, 2026
5-Bromopyrimidine → HCID 21876226, compound
https://huagongshe.com/reaction/858539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromopyrimidine | HCID 78344 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21875769 | HCID 21875769 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 21876226 | HCID 21876226 | 50.3% |
Reaction Steps
To a solution of 2-{4-[2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzimidazol-1-yl]phenyl}ethanol (step 1, 100 mg, 0.26 mmol) and 5-bromopyrimidine (45 mg, 0.28 mmol) in 1,2-dimethoxyethane (3.5 ml) was added sat. NaHCO3 aq. (1.2 ml) and Pd(PPh3)4 (60 mg, 0.05 mmol). This mixture was stirred at 70° C. for 17 h. The reaction mixture was diluted with water and extracted with CH2Cl2 (3×10 ml). The organic layer was dried (MgSO4) and concentrated to give light brown oil. This mixture was purified by SiO2 preparative TLC (CH2Cl2/methanol=10/1) to afford 45 mg (50%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07148234B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-f03084a5f07e427db74a344451403dca |
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| Source note | uspto-grants-2006_12 |
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