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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868601Generated: October 29, 2026

1-Phenylpiperazine → HCID 11591652, compound

https://huagongshe.com/reaction/1868601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantHCID 86236611HCID 86236611—
SolventMethanolHCID 887—
ProductHCID 11591652HCID 11591652—

Reaction Steps

3′,4′-Dimethoxy-7-(2,3-epoxy-propoxy)-flavone, 33 (300 mg, 0.85 mmol) and 1-phenyl piperazine (0.13 mL, 0.85 mmol) in dry methanol (60 mL) were reacted in a similar manner to that described under 34 to afford 47. Yield 410 mg (94%); mp 191-193° C.; MS (FAB) 517 (M++1); IR (KBr) 3416, 1627; 1H NMR (200 MHz, CDCl3) δ 8.16 (d, J=9.5 Hz, 1H), 7.54 (dd, J=8.3 Hz, 2.1 Hz, 1H), 7.34 (d, J=1.9 Hz, 1H), 7.31-7.23 (m, 2H), 7.04-6.87 (m, 6H), 6.70 (s, 1H), 4.21-4.16 (m, 3H), 3.99 (s, 3H), 3.97 (s, 3H), 3.28 (t, J=4.8 Hz, 4H), 2.90-2.71 (m, 2H), 2.71-2.65 (m, 4H). Analysis Calcd for C30H32N2O6: C, 69.75; H, 6.24; N, 5.42. Found: C, 69.96; H, 6.57; N, 5.51.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635779B2
Source datasetuspto-grants-2009_12
ORD IDord-39cb3916a3594163858beae223fdcfcc
Source noteuspto-grants-2009_12