HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411526Generated: October 25, 2026
Potassium Carbonate → 4-({3-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]propyl}amino)benzonitrile
https://huagongshe.com/reaction/411526
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine | HCID 18541030 | — |
| Reactant | 3-(4-Cyanoanilino)propyl 4-methylbenzenesulfonate | HCID 21867652 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-({3-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]propyl}amino)benzonitrile | HCID 18540907 | 65.5% |
Reaction Steps
A mixture of 3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine (Preparation B; 4.0 g, 17.4 mmol), 3-(4-cyanoanilino)propyl 4-methyl-benzenesulfonate (Preparation G(ii); 5.74 g, 17.4 mmol), and potassium carbonate (2.40 g, 17.4 mmol) in DMF (85 mL) was heated at 90° C. under nitrogen overnight. The mixture was partitioned with water (200 mL) and diethyl ether (150 mL). The aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with brine (2×30 mL), dried (Na2SO4), filtered and then concentrated in vacuo. The residue was chromatographed on silica gel, eluting with dichloromethane:methanol (98:2), to afford 3.40 g (50%) of the sub-title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06559162B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-159d2fdcc8c34753ace01f967dbd9955 |
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| Source note | uspto-grants-2003_05 |
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