HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-methanesulfonyl-N-(1-phenyl-4-piperidyl)spiro[indoline-3,4'-piperidine]-1'-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(Methylsulfonyl)spiro[indoline-3,4'-piperidine] hydrochloride | HCID 21956084 | — |
| Reactant | HCID 22936218 | HCID 22936218 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-methanesulfonyl-N-(1-phenyl-4-piperidyl)spiro[indoline-3,4'-piperidine]-1'-carboxamide | HCID 22936223 | 31.6% |
Reaction Steps
1-Methanesulfonyl-spiro[indoline-3,4′-piperidine] hydrochloride (37 mg) and triethylamine (170 μL) were added to a solution of phenyl N-(1-phenyl-4-piperidyl)carbamate (36 mg) in chloroform (3 mL), and the mixture was heated to reflux for 15 hours. The reaction mixture was poured into saturated aqueous sodium bicarbonate and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was crystallized from diethyl ether to give the title compound (18 mg) as a colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205417B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-36c83ac409744c73b3f00b96ca188e3e |
| Source note | uspto-grants-2007_04 |