HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene, (3-bromopropoxy)- → Aclidinium Bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene, (3-bromopropoxy)- | HCID 68522 | — |
| Reactant | (R)-Quinuclidin-3-yl 2-hydroxy-2,2-di(thiophen-2-yl)acetate | HCID 44232927 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Aclidinium Bromide | HCID 11519741 | 90% |
Reaction Steps
0.6 mmol of 2-hydroxy-2,2-dithien-2-ylacetic acid 1-azabicyclo[2.2.2]oct-3(R)yl ester are suspended in 4 ml of CH3CN and 6 ml of CHCl3. 0.48 ml of 3-phenoxypropyl bromide were added to the resulting suspension and the mixture was stirred for 72 h at room temperature in an inert atmosphere. The solvents were subsequently evaporated to yield (90%) of 3(R)-(2-hydroxy-2,2-dithien-2-ylacetoxy)-1-(3-phenoxypropyl)-1-azoniabicyclo[2.2.2]octane bromide. The product is isolated by filtration at room temperature and the level of 3-phenoxypropyl bromide is determined to be 117 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044205B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-a6fe5cd3973e4a57ac27ed7cd670dca0 |
| Source note | uspto-grants-2011_10 |