HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(1-Azabicyclo[2.2.2]oct-3-yl)-4-iodo-3-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Quinuclidine, 3-amino-, dihydrochloride | HCID 197853 | — |
| Reactant | 4-Iodo-3-nitrobenzoyl chloride | HCID 58932935 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(1-Azabicyclo[2.2.2]oct-3-yl)-4-iodo-3-nitrobenzamide | HCID 58932946 | 22.5% |
Reaction Steps
A solution of 3.08 g (24.4 mmol) of 3-aminoquinuclidine dihydrochloride, 7.60 g (24.4 mmol) of 4-iodo-3-nitrobenzoyl chloride, 9.88 g (97.6 mmol) of triethylamine in 150 ml of DMF was stirred at room temperature overnight. The solvent was distilled off in a rotary evaporator, the residue was taken up in 200 ml of dichloromethane, and 200 ml of a saturated sodium bicarbonate solution were added. The organic phase was dried over sodium sulfate, and the solvent was distilled off in vacuo. 2.20 g (22.5%) of the desired title compound were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07256288B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-19bae567823a440c9d3c24ed90770633 |
| Source note | uspto-grants-2007_08 |