HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 5-Chloro-2,3-dihydro-7-[3-(4-piperidinyl)-1,2,4-oxadiazol-5-yl]-4-benzofuranamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 4-[5-(4-amino-5-chloro-2,3-dihydro-7-benzofuranyl)-1,2,4-oxadiazol-3-yl]-1-piperidinecarboxylate | HCID 54520153 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 5-Chloro-2,3-dihydro-7-[3-(4-piperidinyl)-1,2,4-oxadiazol-5-yl]-4-benzofuranamine | HCID 53834017 | 64% |
Reaction Steps
A mixture of intermediate 3 (10 g) and potassium hydroxide (14 g) in 2-propanol (200 ml) was stirred and refluxed for 6 hours. The reaction mixture was cooled and the solvent evaporated. Water was added to the residue and evaporated again. The residue was stirred in water and the resulting precipitate was filtered off, washed with water and purified by column chromatography on silica gel (eluent: CH2Cl2 /(CH3 OH/NH3) 90/10). The pure fractions were collected and the solvent evaporated, yielding 5.14 g (64%) of 5-chloro-2,3-dihydro-7-[3-(4-piperidinyl)-1,2,4-oxadiazol-5-yl]-4-benzofuranamine (intermediate 4; mp. 219.0° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05854261 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-8aef11a8fd604f708d8bf66beddfaf94 |
| Source note | uspto-grants-1998_12 |