HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281250Generated: November 1, 2026
Triethylamine → N-(2-(4-bromophenyl)propan-2-yl)-2-(quinuclidin-3-yl)acetamide
https://huagongshe.com/reaction/2281250
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 2-(4-Bromophenyl)propan-2-amine | HCID 23009116 | — |
| Reactant | 2-(Quinuclidin-3-yl)acetic acid hydrochloride | HCID 23024147 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-(4-bromophenyl)propan-2-yl)-2-(quinuclidin-3-yl)acetamide | HCID 68327949 | 76% |
Reaction Steps
To a solution of 2-(quinuclidin-3-yl)acetic acid hydrochloride (0.97 g, 4.7 mmol) in DMF (30 mL) was added HATU (1.79 g, 4.72 mmol), 2-(4-bromophenyl)propan-2-amine (1.0 g, 4.7 mmol), and triethylamine (3.9 mL, 28 mmol). The resulting mixture was stirred at 60° C. for 16 h. The mixture was concentrated in vacuo, diluted with EtOAc and washed with brine. The organic layer was dried over Na2SO4 and evaporated to afford crude product, which was purified by silica gel column chromatography (EtOAc/methanol 50/1 to 3/1) to obtain N-(2-(4-bromophenyl)propan-2-yl)-2-(quinuclidin-3-yl)acetamide as a yellow solid (1.3 g, 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139580B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-15844f54be8346cc81bc8d0aaeb2204f |
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| Source note | uspto-grants-2015_09 |
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