Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 13-cyclohexyl-6-{[2-(dimethylamino)ethyl]amino}-6,7-dihydro-5H-indolo[2,1-a][2]benzazepine-10-carboxylic acid | HCID 11704967 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68698620 | HCID 68698620 | — |
Reaction Steps
Methyl 13-cyclohexyl-6-{[2-(dimethylamino)ethyl]-amino}-6,7-dihydro-5H-indolo[2,1-a][2]benzazepine-10-carboxylate (prepared as in Example 5, Step 4) was dissolved in DCM (0.07 M) and pH adjusted to 6 with AcOH; 37% aq HCHO and, after half an hour NaCNBH3 (3 eq), were added and the mixture was stirred at RT overnight. The reaction mixture was diluted with EtOAc and washed with 1N NaOH and brine, dried and evaporated affording methyl 13-cyclohexyl-6-{[2-(dimethylamino)ethyl][(methyl) amino]}-6,7-dihydro-5H-indolo[2,1-a][2]benzazepine-10-carboxylate. Hydrolysis of the foregoing methyl ester was done with 1M aqueous KOH (6 eq) in dioxane (0.IM) at 60 ° C.; the reaction was complete in 2 h, and the title compound was obtained in 20% yield after RP-HPLC purification and lyophilisation (Conditions: Column: Waters X-TERRA MS C18, 10 micron, 19×150 mm; Gradient: A: H2O+0.1% TFA; B: MeCN+0.1% TFA; 75% A isocratic for 3 min, linear to 20% A in 12 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662809B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-504ad893b1f44458aae91d50b280e434 |
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| Source note | uspto-grants-2010_02 |
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