HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 67056740, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(Pyridin-4-yl)piperidine-4-carboxylic acid | HCID 1268289 | — |
| Reactant | HCID 18442849 | HCID 18442849 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67056740 | HCID 67056740 | — |
Reaction Steps
1-(4-Pyridyl)piperidine-4-carboxylic acid (Tetrahedron, 1998, Vol. 44, p. 7095) (206 mg) was suspended in dichloromethane (50 ml), thionyl chloride (144 μl) was added under ice cooling, and the mixture was stirred for 30 minutes. After triethylamine (969 μl) was added to the reaction mixture, (±)-cis-N-[(5-chloroindol-2-yl)carbonyl]-1,2-cyclohexanediamine hydrochloride (328 mg) was added, and the mixture was stirred at room temperature for 30 minutes. After the reaction mixture was concentrated under reduced pressure, and water was added to the residue, the solution was concentrated under reduced pressure, and precipitate deposited was collected by filtration to obtain the title compound (310 mg) as a pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935824B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-392e4b6d9b5f4856bf4b0ebc5342ec07 |
| Source note | uspto-grants-2011_05 |