HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879498Generated: October 30, 2026
Water → 5-Bromo-1-methyl-3-(1,2,3,6-tetrahydro-1-methyl-4-pyridinyl)-1H-pyrrolo[2,3-b]pyridine
https://huagongshe.com/reaction/879498
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)boronic acid | HCID 53407231 | — |
| Reactant | 5-bromo-3-iodo-1-methyl-1H-pyrrolo[2,3-b]pyridine | HCID 59812077 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Bromo-1-methyl-3-(1,2,3,6-tetrahydro-1-methyl-4-pyridinyl)-1H-pyrrolo[2,3-b]pyridine | HCID 86700315 | — |
Reaction Steps
To a solution of 5-bromo-3-iodo-1-methyl-1H-pyrrolo[2,3-b]pyridine (180 mg, 0.534 mmol) and 1-methyl-1,2,3,6-tetrahydropyridin-4-boronic acid (155 mg, 0.694 mmol) in dioxane (5.4 mL, degassed) was added tetrakis(triphenylphosphine)palladium(0) (75 mg, 0.064 mmol), K2CO3 (369 mg, 2.67 mmol) and water (1.8 mL, degassed). The reaction mixture was heated at 40° C. for 15 h, cooled and partitioned between ethyl acetate and brine. The organic layer was separated, dried over Na2SO4, filtered and concentrated to give crude which was purified by chromatographic column to afford the desired product. LCMS-ESI+: calc'd for C14H16BrN3: 306.2 (M+H+); Found: 306.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987250B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-607750cc09e944d38a82ea5260d842d9 |
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| Source note | uspto-grants-2015_03 |
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