HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → N-(3-tert-butoxycarbonylaminopropyl)-4-cyano-4-(o-tolyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-butyl N-(3-bromopropyl)carbamate | HCID 4460490 | — |
| Reactant | 4-o-Tolylpiperidine-4-carbonitrile | HCID 10176570 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(3-tert-butoxycarbonylaminopropyl)-4-cyano-4-(o-tolyl)piperidine | HCID 21712249 | — |
Reaction Steps
A solution of 4-cyano-4-(o-tolyl)piperidine (5.00 g, 24.9 mmol) and 1-(tert-butoxycarbonylamino)-3-bromopropane (16, 6.55 g, 27.5 mmol) in DMF (100 mL) was treated with diisopropylethylamine (4.50 mL, 25.8 mmol) at room temperature. The resulting mixture was stirred at room temperature (3 d). The solvent was removed in vacuo and the residue dissolved in dichloromethane and sodium bicarbonate solution. The aqueous layer was extracted with two additional portions of dichloromethane and the combined organic extracts were washed with brine, dried over Na2SO4, and concentrated under reduced pressure. Flash chromatography on silica gel (5% methanol/dichloromethane) afforded the title compound (25).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06274583B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-147422ddf5a84e54949323a0cc52a38b |
| Source note | uspto-grants-2001_08 |