Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridin-3-yl)methyl-10,11-dihydro-5H-dibenzo[b,f]azepine | HCID 19970872 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18998700 | HCID 18998700 | 64% |
Reaction Steps
[step 2] 2-(2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridin-3-yl)methyl-10,11-dihydro-5H-dibenzo[b,f]azepine (55.4 g, 145 mmol) obtained in step 1 was dissolved in acetic acid (500 mL) and the solution was added with potassium cyanide (11 g, 169 mmol) and paraformaldehyde (4.6 g, 152 mmol) at 10° C., followed by stirring at room temperature for 24 hr. The mixture was added to a mixed solution of 10 mol/L aqueous sodium hydroxide solution (900 mL), ice (1 L) and dichloromethane (1 L). The organic layer was washed with 0.1 mol/L aqueous sodium hydroxide solution and brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate/triethylamine=10/10/1) to give 5-cyanomethyl-2-(2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridin-3-yl)methyl-10,11-dihydro-5H-dibenzo[b,f]azepine (39.0 g, 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242151B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-b891e32051c44353b53a080a07e9c40e |
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| Source note | uspto-grants-2012_08 |
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