HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449899Generated: November 1, 2026
Potassium Carbonate → N,N-dimethyl-4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxybenzamide
https://huagongshe.com/reaction/1449899
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazole | HCID 849421 | — |
| Reactant | N,N-dimethyl4 bromopropoxy-3-methoxybenzamide | HCID 10358359 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N,N-dimethyl-4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxybenzamide | HCID 10049666 | — |
Reaction Steps
A stirred mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (3.9 g, 17.7 mmol), N,N-dimethyl-4-bromopropoxy-3-methoxybenzamide (5.54 g, 17.5 mmol) and K2CO3 (3 g) in acetonitrile (250 ml) was heated at reflux for one hour. At the end of the reaction, the insolubles were filtered and washed with dichloromethane. The solvent was removed on a rotary evaporator. The residue was purified by flash chromatography over a silica gel column. The product thus obtained as an oil weighed 7 g. Crystallization from hot ethanol (45 ml) afforded analytically pure N,N-dimethyl-4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxybenzamide, 3.95 g, 50%, as light yellow crystals, m.p.=126°-127° C. ANALYSIS: Calculated for C25H30FN3O4 : 65.92%C 6.64%H 9.22%N Found: 65.76%C 6.64%H 9.14%N
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05599821 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-48ba50b8f3794fdc863e6f6fa133d436 |
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| Source note | uspto-grants-1997_02 |
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