HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-1-(4-hydroxyphenyl)ethanone → (R)-3-(2-(benzo[b]thiophen-3-yl)-2-(phenylamino)acetoxy)-1-(2-(4-hydroxyphenyl)-2-oxoethyl)-1-azoniabicyclo[2.2.2]octane bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-1-(4-hydroxyphenyl)ethanone | HCID 4964 | — |
| Reactant | (R)-quinuclidin-3-yl 2-(benzo[b]thiophen-3-yl)-2-(phenylamino)acetate | HCID 58556957 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (R)-3-(2-(benzo[b]thiophen-3-yl)-2-(phenylamino)acetoxy)-1-(2-(4-hydroxyphenyl)-2-oxoethyl)-1-azoniabicyclo[2.2.2]octane bromide | HCID 54765166 | 66.5% |
Reaction Steps
2-Bromo-1-(4-hydroxyphenyl)ethanone (54.8 mg, 0.25 mmol) was added portionwise to a solution of (R)-quinuclidin-3-yl 2-(benzo[b]thiophen-3-yl)-2-(phenylamino)acetate (C19) (100 mg, 0.25 mmol) in EtOAc (2 ml). The reaction mixture was stirred at room temperature overnight. The precipitate was filtered and washed with ethylacetate and then it was triturated with CH3CN to obtain (R)-3-(2-(benzo[b]thiophen-3-yl)-2-(phenylamino)acetoxy)-1-(2-(4-hydroxyphenyl)-2-oxoethyl)-1-azoniabicyclo[2.2.2]octane bromide (101 mg, 65.3% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629160B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-ab0be06222c249a88351b245d17b5152 |
| Source note | uspto-grants-2014_01 |