HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Chloroacetyl)thiophene → HCID 86672928, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Chloroacetyl)thiophene | HCID 2757925 | — |
| Reactant | HCID 70673881 | HCID 70673881 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86672928 | HCID 86672928 | 72.7% |
Reaction Steps
2-Chloro-1-(thiophen-2-yl)ethanone (12.0 mg, 0.07 mmol) was added to a solution of (4-methoxyphenyl)(phenyl)methyl(R)-quinuclidin-3-ylcarbamate (22.0 mg, 0.06 mmol, prepared as in example 3) in ethyl acetate (2 ml). The reaction was stirred at room temperature for two days. The reaction was evaporated to dryness. The crude was purified by flash chromatography (DCM/MeOH=95/5) to obtain (3R)-3-(((4-methoxyphenyl)(phenyl)methoxy)carbonylamino)-1-(2-oxo-2-(thiophen-2-yl)ethyl)-1-azoniabicyclo[2.2.2]octane chloride (23 mg, mixture of diastereoisomers).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08604015B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-3687e6c7d1684c47b3c5ee1fcefcfa57 |
| Source note | uspto-grants-2013_12 |