HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Azetidin-1-yl(7-(piperazin-1-yl)benzofuran-2-yl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Azetidin-1-yl(7-(4-benzylpiperazin-1-yl)benzofuran-2-yl)methanone | HCID 59636710 | — |
| Product | Azetidin-1-yl(7-(piperazin-1-yl)benzofuran-2-yl)methanone | HCID 59636763 | — |
Reaction Steps
The compound was prepared according to the procedure disclosed in Example 39d starting from azetidin-1-yl(7-(4-benzylpiperazin-1-yl)benzofuran-2-yl)methanone (0.52 g, 1.38 mmol) and acetic acid (0.63 mL, 11.1 mmol). A solution of ammonia (3 mL, 7N in MeOH) was added to the mixture after the reaction was complete. The solvent was removed by rotary evaporation. The crude product was purified by flash chromatography (SiO2; gradient 0-10% ammonia (7N in MeOH) in DCM). Yield: 0.36 g (91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859534B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-bf5e8c97bd894bfe8f4be3c7d9d811ef |
| Source note | uspto-grants-2014_10 |