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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111458Generated: October 29, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 3025928, compound

https://huagongshe.com/reaction/1111458

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactanttert-butyl N-(pyrrolidin-3-yl)carbamateHCID 2757234—
Reactant5-Amino-1-cyclopropyl-6,7-difluoro-8-methoxy-1,4-dihydro-4-oxoquinoline-3-carboxylic acidHCID 10566894—
SolventAcetonitrileHCID 6342—
ProductHCID 3025928HCID 302592832.1%

Reaction Steps

A mixture of 5-amino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid (90 mg), 3-t-butoxycarbonylaminopyrrolidine (115 mg), DBU (50 mg) and anhydrous acetonitrile (4 ml) was refluxed for 20 hours. After cooling, the resulting precipitate was collected by filtration and added to concentrated hydrochloric acid-methanol (1:1, 2 ml). The mixture was stirred for 10 minutes at room temperature, then neutralized with concentrated aqueous ammonia, and the precipitate was collected by filtration. A solution of the precipitate in cold water was acidified with concentrated hydrochloric acid below pH 1 and allowed to stand in a refrigerator. The resulting precipitate was collected by filtration and washed with cold diluted aqueous hydrochloric acid to give the title compound (35 mg) as yellow needles, mp 254°-257° C. (decompd.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980470
Source datasetuspto-grants-1990_12
ORD IDord-5f1674ea3d594c20bfbdabac12cef03e
Source noteuspto-grants-1990_12