Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1-[2-(2-Hydroxyethoxy)ethyl]piperazine | HCID 139436 | — |
| Reactant | HCID 86711153 | HCID 86711153 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86711155 | HCID 86711155 | — |
Reaction Steps
To a solution of 11-chloro-dibenzo[b,f][1,4]thiazepine-3-carboxylic acid amide, prepared as described in the previous step, (0.40 g) in DMF (1.5 mL) and toluene (1.5 mL) was added 2-(2-piperazin-1-yl-ethoxy)-ethanol (0.50 g, 2.9 mmol). The solution was heated in a 110° C. oil bath under nitrogen for 5 hours, concentrated, and purified (silica gel, 2-5% methanol-dichloromethane containing ammonia eluent) to give the title compound as an off white solid. LC-MS: m/z 427 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09304126B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-c1fb51c7072f4d28a78a04e74c217f97 |
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| Source note | uspto-grants-2016_04 |
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