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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877957Generated: October 31, 2026

N,N,N',N'-Tetramethylethylenediamine → 5-(2-Bromophenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine

https://huagongshe.com/reaction/1877957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-(2-Bromobenzyl)-5-(3-chloropropyl)-1H-imidazoleHCID 58827085—
SolventTetrahydrofuranHCID 8028—
Product5-(2-Bromophenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridineHCID 58827122—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314097B2
Source datasetuspto-grants-2012_11
ORD IDord-2711f91742b84b739a17c55f961d2166
Source noteuspto-grants-2012_11