HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619117Generated: October 26, 2026
Sodium Bicarbonate → 6-fluoro-1-methyl-4-[2-[4-(thieno[3,2-c]pyridine-4-yl)-1-piperazinyl]ethyl]-2(1H)-quinolone hydrochloride
https://huagongshe.com/reaction/619117
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-(Piperazin-1-yl)thieno[3,2-c]pyridine | HCID 10966027 | — |
| Reactant | 4-(2-chloroethyl)-6-fluoro-1-methyl-2(1H)-quinolone | HCID 21846043 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-fluoro-1-methyl-4-[2-[4-(thieno[3,2-c]pyridine-4-yl)-1-piperazinyl]ethyl]-2(1H)-quinolone hydrochloride | HCID 21846039 | 27% |
Reaction Steps
1.4 g (5.8 mmol) of 4-(2-chloroethyl)-6-fluoro-1-methyl-2(1H)-quinolone are added to a mixture of 1.3 g (5.9 mmol) of 4-(1-piperazinyl)thieno[3,2-c]pyridine and 0.50 g (5.95 mmol) of sodium hydrogen carbonate in 20 ml of acetonitrile, and the reaction medium is heated to 55-60° C. for 18 hours. The solvent is evaporated off and the residue is taken up in 100 ml of dichloromethane. It is washed with saturated aqueous sodium bicarbonate solution and then with water. The organic phase is dried over sodium sulphate and filtered and the filtrate is condensed. The crude product is purified by flash chromatography on silica, eluting with a methanol/dichloromethane (5:95) mixture containing traces of aqueous ammonia. 0.70 g of the expected product is obtained in base form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05958924 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-0176029c30724412b685e2b0d7b42484 |
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| Source note | uspto-grants-1999_09 |
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