Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | HCID 23328936 | HCID 23328936 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20470725 | HCID 20470725 | — |
Reaction Steps
With stirring, 21.8 g (0.1 mole) of 10-cyano-5H-dibenz[b,f]azepine are added to a solution of 19.8 g (0.2 mole) of phosgene in 700 ml of absolute toluene. The mixture is then stirred for 30 hours at 50°-53° C. and subsequently completely concentrated in a rotary evaporator, affording as residue crude 10-cyano-5H-dibenz[b,f]azepine-5-carbonyl chloride with a melting point of 148°-153° C. With stirring, the crude product is dissolved at 70° C. in 600 ml of absolute ethanol. Ammonia gas is then introduced into this solution in the course of 2 hours while constantly keeping the reaction mixture under reflux. The reaction mixture is then concentrated in a rotary evaporator and the residue is washed and dried. Recrystallisation from toluene yields 10-cyano-5H-dibenz[b,f]azepine-5-carboxamide with a melting point of 212°-215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04235895 |
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| Source dataset | uspto-grants-1980_11 |
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| ORD ID | ord-9c59dc7e22534723a26de7547fe072dc |
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| Source note | uspto-grants-1980_11 |
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