HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → HCID 68575388, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | HCID 68574648 | HCID 68574648 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68575388 | HCID 68575388 | — |
Reaction Steps
A solution of 139.8 mg of benzyl 4-[4-(5-bromopyrimidin-2-yloxy)phenyl]-3-hydroxy-5-[4 -(3-methoxypropyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]piperidine-1-carboxylate in 0.5 ml of dichloromethane is added to a mixture of 0.232 ml of boron trifiuoride etherate and 0.4 ml of ethanethiol. The reaction mixture is stirred at room temperature under argon for 20 hours. The solvent is then evaporated off, and 2 ml of water are added to the residue. The aqueous phase is extracted three times with 5 ml of ethyl acetate each time. The combined organic phases are dried with sodium sulphate, filtered and evaporated. The title compound is obtained as a beige wax from the residue by flash chromatography (SiO2 60F).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07799779B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-893df30155474e6a8cc39cf51489f9bd |
| Source note | uspto-grants-2010_09 |