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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920705Generated: October 29, 2026

Piperazine → HCID 59526801, compound

https://huagongshe.com/reaction/1920705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantHCID 58420505HCID 58420505—
ReactantHCID 59687293HCID 59687293—
ProductHCID 59526801HCID 59526801—

Reaction Steps

The title compound is prepared from piperazine and ethyl 1-cyclopropyl-8-(difluoromethoxy)-6,7-difluoro-2-(methylsulfonyl)-4-oxo-1,4-dihydroquinoline-3-carboxylate using a procedure analogous to that describing the preparation of (R)-ethyl 7-(3-(2-aminopropan-2-yl)pyrrolidin-1-yl)-1-cyclopropyl-6-fluoro-8-methoxy-2-(methylsulfonyl)-4-oxo-1,4-dihydroquinoline-3-carboxylate. (See US 2008071086, and Hashimoto, et al., 2007) 1H NMR (CDCl3): δ 0.30-0.33 (m, 1H), 0.84-0.88 (m, 1H), 0.99-1.04 (m, 1H), 1.20-1.25 (m, 1H), 1.38 (t, J=7.2 Hz, 3H), 2.95-3.21 (m, 6H), 3.44 (s, 3H), 3.51-3.58 (m, 2H), 4.13-4.18 (m, 1H), 4.36-4.48 (m, 2H), 6.54 (dd, J=76.0 Hz, 73.0 Hz, 1H), 7.72 (d, J=12.0 Hz, 1H). 19F NMR (CDCl3): δ −120.4 (s, 1F), −82.1 (s, 2F). LCMS: m/z calcd for C21H24F3N3O6S ([M]+) 503. found ([M+H]+) 504.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173636B2
Source datasetuspto-grants-2012_05
ORD IDord-7c851e368ced41138724251d124f70a1
Source noteuspto-grants-2012_05