Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(5H-Dibenzo(a,d)cyclohepten-5-ylidene)piperidine | HCID 159718 | — |
| Reactant | HCID 86595916 | HCID 86595916 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86594133 | HCID 86594133 | — |
Reaction Steps
475 mg (2.93 mmol) of N,N′-carbonyldiimidazole was dissolved in 10 ml of anhydrous tetrahydrofuran. 0.45 ml (3.29 mmol) of triethylamine was added to the obtained solution, and they were stirred at room temperature for 10 minutes. The reaction mixture was cooled with ice, and 460 mg (2.74 mmol) of glycine t-butyl hydrochloride was added dropwise to the mixture during a period of about 10 minutes, and they were stirred at room temperature for 1 hour. After cooling with ice, 500 mg (1.83 mmol) of 4-(5H-dibenzo[a,d][7]annulen-5-ylidene)piperidine was added to the resultant mixture, and they were stirred at room temperature overnight. Water was added to the reaction mixture. After extracting with ethyl acetate followed by drying over anhydrous magnesium sulfate, the product was concentrated under reduced pressure. The residue thus obtained was purified by the silica gel chromatography (dichloromethane: methanol=95:5 to 2:3) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713957B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-4fe5f546bb1642ab883507649540bb1e |
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| Source note | uspto-grants-2010_05 |
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