HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868065Generated: October 29, 2026
Acetic Acid → 7-(2-Aminopyrimidin-4-yl)-1-ethyl-6-fluoro-4-oxo-quinoline-3-carboxylic acid
https://huagongshe.com/reaction/868065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 7-(2'-Dimethylaminoethenyl)carbonyl-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid ethyl ester | HCID 54057449 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 7-(2-Aminopyrimidin-4-yl)-1-ethyl-6-fluoro-4-oxo-quinoline-3-carboxylic acid | HCID 461439 | 35.9% |
Reaction Steps
To 900 mg (2.5 mmol) of the 7-(2'-dimethylaminoethenyl)carbonyl-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid ethyl ester in 15 ml of t-butanol at 50° C. was added 580 mg (2.5 eq) of guanidine hydrochloride that had been previously treated with 1.35 g (5 eq) of potassium t-butoxide at 50° C. in t-butanol for 30 minutes. The final mixture was stirred for 24 hours at 60° C. It was poured into 8% aqueous acetic acid and extracted into chloroform. The chloroform was extracted three times with water. The chloroform was dried magnesium sulfate and concentrated. The residue was purified by column chromatography and gave 295 mg of 7-(2-amino-4-pyrimidinyl)-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, mp 245°-247° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04777175 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-2701e33c7f8c42e194ea98084511113f |
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| Source note | uspto-grants-1988_10 |
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