HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[1-(2-pyridinyl)-4-piperidinyl]-1H-imidazole-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 1-(Pyridin-2-yl)piperidin-4-amine dihydrochloride | HCID 66631096 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[1-(2-pyridinyl)-4-piperidinyl]-1H-imidazole-1-carboxamide | HCID 21978278 | — |
Reaction Steps
A suspension comprising CDI (2.29 g, 14 mmol) and triethylamine (3.8 ml, 27 mmol) in dry DCM (20 ml) is treated portionwise over 5 minutes with 3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-ylamine dihydrochloride (prepared using the procedure described in international patent application WO 01/94368) (2.88 g, 13 mmol). The reaction mixture is stirred at room temperature for 4.5 hours to yield the title compound as a 0.43 M solution in DCM.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318750B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-ea8101c5af7b4100b3179df2bc91826c |
| Source note | uspto-grants-2012_11 |