HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457215Generated: October 30, 2026
Potassium Iodide → HCID 66759130, compound
https://huagongshe.com/reaction/457215
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | HCID 7004871 | HCID 7004871 | — |
| Reactant | 2-[5-(3-Bromo-propylidene)-5,1 1-dihydro-10-oxa-1-aza-dibenzo[a,d]cyclohepten-7-yl]-propan-2-ol | HCID 66685999 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 66759130 | HCID 66759130 | — |
Reaction Steps
To a solution of 4-(4-chloro-phenyl)-3-(R)-methyl-piperazine (0.2 g, 0.95 mmol) in isopropanol (20 mL) was added 2,6-lutidine (0.11 mL, 0.94 mmol) and catalytic potassium iodide. This mixture was heated to 80° C. and then treated with 2-[5-(3-bromo-propylidene)-5,11-dihydro-10-oxa-1-aza-dibenzo[a,d]cyclohepten-7-yl]-propan-2-ol (0.24 g, 0.63 mmol), added in portions over 2 h. The solution was then stirred at 80° C. for an additional 20 h. The reaction was concentrated in vacuo and purified by flash chromatography (100% dichloromethane to 2% methanol/dichloromethane) to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07186729B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-065f62594bbe45118c580b58799bd336 |
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| Source note | uspto-grants-2007_03 |
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