HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265249Generated: October 28, 2026
Benzoyl isothiocyanate → HCID 9886701, compound
https://huagongshe.com/reaction/265249
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | 93107-09-6 | HCID 67233309 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9886701 | HCID 9886701 | — |
Reaction Steps
[6R-[6a,7b]]-3-[[[(3-Carboxy-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1-quinolinyl)-4-piperazinyl]iminomethyl]thio methyl]-8-oxo-7-[(2-thienylacetyl)amino]-5-thia-1-azabicyclo [4.2.0]oct-2-ene-2-carboxylic acid sodium salt, of the following formula ##STR330## according to this invention, is made as follows. A solution of benzoyl isothiocyanate 10.92 g) in THF (20 ml) is added to a mixture of ciprofloxacin sodium salt (2.0 g) in THF (300 ml), and the reaction is stirred for 20 hours. The reaction is concentrated to dryness and the residue is triturated with acetone. The resultant benzoylurea is added to a preheated at approximately 80° C. (176° F.) solution of 5% aqueous NaOH and the reaction is stirred for 30 minutes. The mixture is cooled to approximately 5° C. (41° F.) and acidified with 1N HCl. The solid is collected by filtration and recrystallized from DMF to yield 7-[4-(aminothioxomethyl)-1-piperazinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05648346 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-25c4c72ec3424d0f858a18fcde2bf6f1 |
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| Source note | uspto-grants-1997_07 |
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