HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458898Generated: October 25, 2026
Water → 5-(2,5-Dimethoxybenzylamino)-6-diphenylmethyl-1-azabicyclo-[2.2.2]octane-3-carboxamide
https://huagongshe.com/reaction/1458898
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 2,5-Dimethoxybenzenemethanamine | HCID 18652 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | N,N-Dimethyl-6-diphenylmethyl-5-oxo-1-azabicyclo[2.2.2]-octane-3-carboxamide | HCID 22097572 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(2,5-Dimethoxybenzylamino)-6-diphenylmethyl-1-azabicyclo-[2.2.2]octane-3-carboxamide | HCID 19701532 | 19% |
Reaction Steps
A mixture of 48 (1.2 g, 3 mmol), 2,5-dimethoxybenzyl amine (0.6 g, 3.3 mmol) camphor sulfonic acid (45 mg) in toluene (15 ml) was heated at reflux with removal of water for 3 hours and then the solvent was removed. The residue was dissolved in small amount of THF (3 ml) and this solution was added to a solution of sodium triacetoxyborohydride (1.7 g, 8 mmol) in acetic acid (40 ml) at room temperature. The mixture was stirred at room temperature for 3 hours and the solvent was removed. Water was added and the mixture was neutralized with NaHCO3 and extracted with EtOAc three times. The combined extracts were dried over Na2SO4 and concentrated. Recrystallization from MeOH/acetone to give by-product. The mother liquor was concentrated and the residue was purified by recrystallization from MeOH/EtOAc to give 50 (0.27 g, 0.56 mmol, 19%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05852038 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-562fa990bcdc4a8e8c98106cdd4c336c |
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| Source note | uspto-grants-1998_12 |
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