HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471769Generated: October 30, 2026
Isobutylene oxide → 5-(2-Fluoro-4-methanesulfonyl-phenyl)-2-[1-(2-hydroxy-2-methyl-propyl)-piperidin-4-yl]-furo[2,3-c]pyridine
https://huagongshe.com/reaction/1471769
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutylene oxide | HCID 11208 | — |
| Reactant | 5-(2-Fluoro-4-methanesulfonyl-phenyl)-2-piperidin-4-yl-furo[2,3-c]pyridine | HCID 86694575 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(2-Fluoro-4-methanesulfonyl-phenyl)-2-[1-(2-hydroxy-2-methyl-propyl)-piperidin-4-yl]-furo[2,3-c]pyridine | HCID 86694578 | — |
Reaction Steps
1,1-Dimethyloxirane (55 μL) is added to a solution of 5-(2-fluoro-4-methanesulfonyl-phenyl)-2-piperidin-4-yl-furo[2,3-c]pyridine (0.15 g) in methanol (2 mL) and dichloromethane (3 mL) at room temperature. The solution is stirred at 50° C. overnight. The solution is concentrated to give the crude title compound that is used without further purification. LC (method 4): tR=0.98 min; Mass spectrum (ESI+): m/z=447 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012456B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-7806fb0d48b04b89b86de97677c45319 |
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| Source note | uspto-grants-2015_04 |
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