Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 9-Benzyl-3,6-dicyanocarbazole | HCID 21394875 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 178509441 | HCID 178509441 | 25.9% |
Reaction Steps
A slurry of 9-benzyl-3,6-dicyanocarbazole (3.8 g, see Example 3C) and sodium hydride (50% in oil, 1.21 g) in 20 ml of dimethylsulfoxide is treated dropwise with m-trifluoromethylaniline (4.04 g). The reaction mixture is stirred at room temperature for four days and then poured into 500 ml of water and stirred vigorously for two hours. The resultant precipitate is collected by filtration and purified by column chromatography using one liter of silica gel. Elution with dichloromethane and 1% ethyl acetate/dichloromethane yields 1.5 g of 6-cyano-9-(phenylmethyl)-N-[3-(trifluoromethyl)phenyl]- 3-carbazolecarboximidamide. Elution with 20% ethyl acetate/dichloromethane/methanol (2:7:1) yields 2g of the desired diamidine, which is recrystallized from two liters of water containing 10 ml of concentrated hydrochloric acid to yield 1.6 g of the title compound, melting point 210°-220° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04061655 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-1f6717f1e20a45a88bc8f88155aac577 |
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| Source note | uspto-grants-1977_12 |
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