HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 18536489, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 18536348 | HCID 18536348 | — |
| Reactant | tert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylate | HCID 22181157 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18536489 | HCID 18536489 | 95.5% |
Reaction Steps
A solution of 4-(4-aminophenoxy)piperidine-1-carboxylic acid tert-butyl ester (8.21 g), 2-chloromethyl-1-(cyclohexylcarbamoylmethyl)-5-cyanobenzimidazole (9.29 g) and diisopropylethylamine (9.8 ml) in dimethylformamide (93 ml) was stirred at 60° C. for 14 hours. After completion of the reaction, the solvent was evaporated and the obtained residue was extracted with ethyl acetate and washed with water. The organic layer was dried over anhydrous magnesium sulfate and the solvent was evaporated. To the obtained residue were added ethyl acetate and hexane and the precipitated solid was collected by filtration, washed with diisopropyl ether and dried under reduced pressure to give the title compound (15.726 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562828B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-d2199b703c574100a39c0ea2ae99a299 |
| Source note | uspto-grants-2003_05 |