HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744421Generated: October 28, 2026
3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazole → 4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-2-hydroxy-1-propoxy]-3-methoxyphenyl methanone
https://huagongshe.com/reaction/744421
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazole | HCID 849421 | — |
| Reactant | 3-Methoxy-4-(2-oxiranylmethoxy)benzaldehyde | HCID 11344798 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-2-hydroxy-1-propoxy]-3-methoxyphenyl methanone | HCID 18467368 | 89.2% |
Reaction Steps
A stirred mixture of 4-(2,3-epoxypropoxy)-3-methoxyphenyl methanone (4.5 g, 22.5 mmol) and 4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine (5.36 g, 24.3 retool) in isopropyl alcohol (150 ml) was heated at 55° C. for 16 hours. The mixture was cooled and the solvent was removed on a rotary evaporator. The residue was purified by flash chromatography over a silica gel column (SiO2, 80 g; eluted with dichloromethane, DCM, and 1% CH3OH in DCM). The oil thus obtained solidified quickly, weight: 9.47 g. Recrystallization from ethanol and isopropyl ether, then toluene provided 8.6 g (86%) of white crystals, m.p.=107°-108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05559117 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-6b35a197b26e44d8b9752d5c0fd7ac66 |
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| Source note | uspto-grants-1996_09 |
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