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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768359Generated: October 30, 2026

p-(1-Piperazinyl)phenol → HCID 10363170, compound

https://huagongshe.com/reaction/1768359

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-(1-Piperazinyl)phenolHCID 92467—
ReactantHCID 22065976HCID 22065976—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 10363170HCID 10363170—

Reaction Steps

The solution from Example 25C (2 mL) was treated with 4-(1-piperazinyl)phenol (178 mg) in DMSO (1 mL). After 72 hours, the mixture was concentrated under a stream of nitrogen gas and the residue recrystallized from DMSO:methanol (1:1) to provide the title compound. 1H NMR (CDCl3, 300 MHz) δ 2.81 (4H, t, J=4.8 Hz), 3.18 (4H, J=4.8 Hz), 3.95 (s, 2H), 6.78 (2H, d, J=9 Hz), 6.90 (2H, J=9 Hz), 7.48 (1H, s), 8.38 (1H, m), 8.80 (1H, m). MS (DCI/NH3) m/z 394 (M+H)+. Anal. Calcd for C19H18N3F3OS: C, 56.72; H, 4.76; N, 10.44. Found: C, 56.43; H, 4.50; N, 10.35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235661B2
Source datasetuspto-grants-2007_06
ORD IDord-306e9df59e2a40e2a9e93ec44ce66bcd
Source noteuspto-grants-2007_06