HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588337Generated: October 29, 2026
Potassium Carbonate → (3R)-N-(4'-Nitrobiphenyl-4-yl)quinuclidine-3-carboxamide hydrochloride
https://huagongshe.com/reaction/588337
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Amino-4'-nitrobiphenyl | HCID 14593 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | (3R)-Quinuclidine-3-carbonyl chloride hydrochloride | HCID 57462844 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (3R)-N-(4'-Nitrobiphenyl-4-yl)quinuclidine-3-carboxamide hydrochloride | HCID 67427704 | — |
Reaction Steps
480 mg (3.50 mmol) of potassium carbonate are added to a mixture, prepared under argon, of 490 mg (2.33 mmol) of (3R)-quinuclidine-3-carbonyl chloride hydrochloride (Example 5A) and 250 mg (1.17 mmol) of 4-amino-4′-nitrobiphenyl in 11 ml of a 10:1 mixture of dioxane and DMF. The reaction mixture is stirred at 100° C. for 18 h and then concentrated. The residue is suspended in methanol and filtered. The filtration residue is washed with water, mixed with 20 ml of a 3:1 mixture of acetonitrile and 1 N hydrochloric acid, again concentrated and dried under high vacuum. The above filtrate is purified by preparative HPLC. The product fractions are concentrated, taken up in 5 ml of a 3:1 mixture of acetonitrile and 1 N hydrochloric acid, again concentrated and dried under high vacuum. 291 mg (61.7% of theory) of the title compound are obtained from the filtration residue, and a further 65 mg (12.4% of theory) are obtained from the filtrate, in this way.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227964B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-be71419077a1481da47f58a334ff99db |
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| Source note | uspto-grants-2016_01 |
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