HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → 5-(p-Bromophenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 1-(p-bromobenzyl)-5-(3-chloropropyl)-1H-imidazole | HCID 14801725 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(p-Bromophenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine | HCID 14097196 | — |
Reaction Steps
A solution of lithium diisopropylamide, prepared at 0° from 0.12 ml of diisopropylamine and 0.33 ml of n-butyllithium (2.5M) in 2 ml of tetrahydrofuran under nitrogen, is added to a solution of 0.13 ml of N,N,N', N'-tetramethylethylene diamine and 0.124 g of 5-(3-chloropropyl)-1-p-bromobenzyl-1H-imidazole in 2 ml of tetrahydroduran at -78°. The reaction mixture is stirred for 3.5 hours, quenched at -78° with saturated ammonium chloride solution and extracted with methylene chloride (3×10 ml). The organic extracts are dried over sodium sulfate and evaporated to yield the title compound (c) which is purified by conversion to the hydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04617307 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-d4eec199eff8407bbe67f0c9314f7515 |
| Source note | uspto-grants-1986_10 |