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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22308Generated: October 26, 2026

1-Phenylpiperazine → 6-methoxy-7-[3-(4-phenyl-1-piperazinyl)propoxy]-2H-1-benzopyran-2-one

https://huagongshe.com/reaction/22308

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantFumarateHCID 5460307—
Reactant3-(chloropropoxy)-6-methoxy-2H-1-benzopyran-2-oneHCID 86748753—
SolventIsopropanolHCID 3776—
Solventtert-Butyl methyl etherHCID 15413—
Product6-methoxy-7-[3-(4-phenyl-1-piperazinyl)propoxy]-2H-1-benzopyran-2-oneHCID 1992767494%

Reaction Steps

Method B (9 h at 70° C.); starting materials: 7-[3-(chloropropoxy)-6-methoxy-2H-1-benzopyran-2-one (see example 69) and 1-phenylpiperazine; yield 94%; fusion point 82° to 83° (from isopropanol and TBME). Fumarate: method E; yield 94%; fusion point 168° to 170° C. (from isopropanol and TBME).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428038
Source datasetuspto-grants-1995_06
ORD IDord-6847489470b44f3c997251298a9f7a2a
Source noteuspto-grants-1995_06