HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Benzyl 2-[({[2-(diisopropylamino)ethyl]amino}carbonyl)amino]ethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl N-(2-aminoethyl)carbamate hydrochloride | HCID 12715871 | — |
| Reactant | N-[2-(diisopropylamino)ethyl]-1H-imidazole-1-carboxamide | HCID 21978296 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 2-[({[2-(diisopropylamino)ethyl]amino}carbonyl)amino]ethylcarbamate | HCID 21978301 | 109.6% |
Reaction Steps
A solution of benzyl 2-aminoethylcarbamate hydrochloride (4.33 g, 18.8 mmol), N-[2-(diisopropylamino)ethyl]-1H-imidazole-1-carboxamide (Preparation 19) (3.73 g, 15.64 mmol) and triethylamine (2.62 ml, 18.8 mmol) in dichloromethane (100 ml) was heated under reflux for 14 hours. The solution was allowed to cool to room temperature and then washed with water (20 ml). The aqueous layer was separated and extracted with more dichloromethane (20 ml). The combined organic layers were dried over anhydrous magnesium sulfate and solvent evaporated under reduced pressure to give the title compound as a yellow oil (6.25 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06753322B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-fd09094a1e5f459c91921fc8190f3e90 |
| Source note | uspto-grants-2004_06 |