HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742425Generated: October 28, 2026
Sodium hydride → 3-(3-Bromo-6,7-dihydro-5H-[1]pyrindin-7-yl)-2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine
https://huagongshe.com/reaction/1742425
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | 3-bromo-7-chloro-6,7-dihydro-5H-cyclopenta[b]pyridine | HCID 67843076 | — |
| Reactant | HCID 178437439 | HCID 178437439 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(3-Bromo-6,7-dihydro-5H-[1]pyrindin-7-yl)-2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine | HCID 67843072 | 13.8% |
Reaction Steps
To a solution of NaH, 60% in oil, (163 mg) in 3 mL of 1,4-dioxane was added 2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine (1.1 gm) at room temperature and stirred for 30 minutes. Then 3-bromo-7-chloro-6,7-dihydro-5H-[1]pyrindine (500 mg, 2.15 mM) in 2 mL of 1,4-dioxane and anhydrous NaBr (442 mg) were added to the solution and the reaction was heated to 100° C. for 24 hours. The reaction was then cooled to room temperature, concentrated to dryness, and extracted into ethyl acetate from water. The organic layers were dried over MgSO4, filtered, and evaporated to dryness. The residue was purified by chromatography on silica gel to yield 110 mg of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05338740 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-0ba5798fcf0c4766be13fff8fba00fe5 |
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| Source note | uspto-grants-1994_08 |
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