Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Viqualine | HCID 3050111 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 69354268 | HCID 69354268 | — |
Reaction Steps
18.4 cm3 of triethylamine were added to a stirred solution of 20.8 g of (3R,4R)-4-[3-(6-methoxyquinolin-4-yl)propyl]-3-vinylpiperidine in 270 cm3 of chloroform, followed, over 1 hour, by a solution of 7.2 cm3 of benzoyl chloride in 50 cm3 of chloroform. After stirring the mixture at a temperature in the region of 20° C. for 1 hour 30 minutes, 100 cm3 of distilled water were added to the reaction mixture. The chloroform phase was separated by settling, washed with 2 times 100 cm3 of water, and then dried over magnesium sulfate. After filtering through paper, the chloroform solution was concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C. 25 g of (3R,4R)-1-benzoyl-4-[3-(6-methoxyquinolin-4-yl)propyl]-3-vinylpiperidine were obtained in the form of a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403610B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-64d1c3be898f4faa845b25165e783e42 |
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| Source note | uspto-grants-2002_06 |
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