HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → HCID 136413216, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 67395701 | HCID 67395701 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 136413216 | HCID 136413216 | — |
Reaction Steps
Boron tribromide (0.14 mL, 1.49 mmol) was added dropwise to a cooled solution of [2-(4-{5-[2-(3,4-dimethoxy-phenyl)-vinyl]-[1,2,4]oxadiazol-3-ylmethyl}-piperidin-1-yl)-ethyl]-dimethyl-amine (compound of Example 23; 0.10 g, 0.25 mmol) in dichloromethane (5 mL) at −78° C. The reaction mixture was warmed to room temperature and stirred for 6 h. The reaction mass was quenched with methanol (2 mL) and the organic solvent was evaporated. The residue obtained was dissolved in 8% methanolic ammonia (5 mL) and the inorganic solid obtained was removed by filtration. The filtrate was concentrated and purified by column chromatography (silica gel, 3% methanol in chloroform) to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629277B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-ae4192ddd75f40dfbe85c5ca675cf90d |
| Source note | uspto-grants-2014_01 |