HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76895Generated: October 29, 2026
N,N,N',N'-Tetramethylethylenediamine → 5-(2-Bromophenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine
https://huagongshe.com/reaction/76895
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 1-(2-Bromobenzyl)-5-(3-chloropropyl)-1H-imidazole | HCID 58827085 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(2-Bromophenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine | HCID 58827122 | — |
Reaction Steps
To a slurry of 1-(2-bromobenzyl)-5-(3-chloropropyl)-1H-imidazole (0.662 g, 2.12 mmol) and TMEDA (0.683 mL, 4.55 mmol) in THF (10 mL) at −78° C. is added LDA (1.8 M in heptane/THF/ethylbenzene, 2.5 mL, 4.5 mmol) and the yellow clear solution is stirred at −78° C. After 3.5 hr, the reaction is quenched by saturated aqueous NH4Cl, and the mixture is partitioned between EtOAc and saturated aqueous NaHCO3. The organic layer is washed with brine, dried and concentrated to give an oil, which is subjected to flash chromatography (silica gel) eluting with MeOH:CH2Cl2 to yield the desired compound. MS (ESI) m/z 277 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835646B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-7322af3dfd524bfab924f8ebf454cd61 |
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| Source note | uspto-grants-2014_09 |
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