HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975334Generated: October 31, 2026
Tert-butyl 5-azaspiro[2.4]heptan-7-ylcarbamate → 7-(7-Tert-butoxycarbonylamino-5-azaspiro[2,4]heptan-5-yl)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
https://huagongshe.com/reaction/1975334
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-butyl 5-azaspiro[2.4]heptan-7-ylcarbamate | HCID 14930995 | — |
| Reactant | 1-Cyclopropyl-6,7-difluoro-2,3-dihydro-4-oxoquinoline-3-carboxylic acid | HCID 15115582 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 7-(7-Tert-butoxycarbonylamino-5-azaspiro[2,4]heptan-5-yl)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid | HCID 15338010 | — |
Reaction Steps
250 mg of 1-cyclopropyl-6,7-difluoro-2,3-dihydro-4-oxoquinoline-3-carboxylic acid and 250 mg of compound 11 were added to 4 ml of dimethyl sulfoxide and the mixture was heated at 120° C. for 2 hours. After cooling, the solvent was removed under reduced pressure and the residue was crystallized by the addition of ethanol. The crystals were collected by filtration. The procedure gave 7-(7-tert-butoxycarbonylamino-5-azaspiro[2,4]heptan-5-yl)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid as a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05286723 |
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| Source dataset | uspto-grants-1994_02 |
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| ORD ID | ord-85a72b319b7e4891bcc6273c1e335d9e |
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| Source note | uspto-grants-1994_02 |
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