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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22342Generated: October 28, 2026

Isopropanol → 2,3-dihydro-7-methoxy-8-[3-(4-phenyl-1-piperidinyl)propoxy]cyclopenta[c][1]benzopyran-4(1H)-one

https://huagongshe.com/reaction/22342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactant4-PhenylpiperidineHCID 69873—
ReactantFumarateHCID 5460307—
Reactant2,3-dihydro-8-[3-(methanesulfonyloxy)propoxy]-7-methoxy-cyclopenta[c][1]-benzopyran-4(1H)-oneHCID 19927662—
SolventEthanolHCID 702—
Product2,3-dihydro-7-methoxy-8-[3-(4-phenyl-1-piperidinyl)propoxy]cyclopenta[c][1]benzopyran-4(1H)-oneHCID 1992764665%

Reaction Steps

Method B (60 h at 25° C.); starting materials: 2,3-dihydro-8-[3-(methanesulfonyloxy)propoxy]-7-methoxy-cyclopenta[c][1]-benzopyran-4(1H)-one (example 82) and 4-phenylpiperidine; yield 65%; fusion point 164°-166° C. (from isopropanol). Fumarate: method E; yield 86%; fusion point 195°-198° C. (from ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428038
Source datasetuspto-grants-1995_06
ORD IDord-dba128891fca4621af94e618a5af991d
Source noteuspto-grants-1995_06