HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl orthoformate → 1-benzyl-4,5-dihydro-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | N-Benzylethylenediamine | HCID 77801 | — |
| Reactant | HCID 69224605 | HCID 69224605 | — |
| Product | 1-benzyl-4,5-dihydro-1H-imidazole | HCID 10877422 | — |
Reaction Steps
As shown in FIG. 9B (Scheme 4), the synthesis of 1-(3-aminopropyl)-3-benzylimidazolidin-2-one (35) will be performed by treating the starting material N1-benzylethane-1,2-diamine with diethoxymethoxyethane to form 1-benzyl-4,5-dihydro-1H-imidazole. The imidazole intermediate will be treated with BuLi (forming a lithiate) followed by quenching with water to form the final intermediate 1-benzylimidazolidin-2-one. Treating the imidazolidinone with NaH followed by Br—(CH2)3—N(SiMe3)2 under reducing conditions will afford the intermediate 35.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07470703B1 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-79d5c8a412904410b706e10077374923 |
| Source note | uspto-grants-2008_12 |