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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923276Generated: November 1, 2026

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

https://huagongshe.com/reaction/923276

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 numberUS09278969B2
Source datasetuspto-grants-2016_03
ORD IDord-4dbe04ba765245c0b8f02b1b0de51b16
Source noteuspto-grants-2016_03