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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249252Generated: October 30, 2026

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

https://huagongshe.com/reaction/2249252

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 numberUS05043450
Source datasetuspto-grants-1991_08
ORD IDord-39aae02ad6c146578a50c6d8d19a580e
Source noteuspto-grants-1991_08