HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → (S)-3-tert-Butoxycarbonylamino-1,1-bis-[3-(3-methoxy-phenyl)-propyl]-piperidinium hydroxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(3-Bromopropyl)-3-methoxybenzene | HCID 138877 | — |
| Reactant | tert-butyl N-[(3S)-piperidin-3-yl]carbamate | HCID 1514171 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (S)-3-tert-Butoxycarbonylamino-1,1-bis-[3-(3-methoxy-phenyl)-propyl]-piperidinium hydroxide | HCID 117856455 | — |
Reaction Steps
(S)-Piperidin-3-yl-carbamic acid tert-butyl ester (2.72 g, 13.6 mmol) and 1-(3-Bromo-propyl)-3-methoxy-benzene (6.6 g, 28.8 mmol), potassium carbonate (2.5 g, 18 mmol) and sodium iodide (4 g, 26.7 mmol) are dissolved in acetonitril (40 ml) and stirred at reflux for 1 day and the solvent is removed under vacuo. The residue is taken up in dichloromethane, filtered through a pad of silica, washed with a mixture of dichloromethane: methanol:conc.ammonia=4:1:0.1 and the filtrate is evaporated. LC (method L): tR=1.30 min; Mass spectrum (ESI+): m/z=497 [M]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096548B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-b8040f7662784d95ac0e1c0337b03704 |
| Source note | uspto-grants-2015_08 |