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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423592Generated: November 1, 2026

HCID 23087242, compound → HCID 66627012, compound

https://huagongshe.com/reaction/2423592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23087242HCID 23087242—
ReactantHCID 66626928HCID 66626928—
ProductHCID 66627012HCID 66627012—

Reaction Steps

Synthesized from [4-methoxy-2-(7-methoxy-3,4-dihydronaphthalen-2-yl)phenyl][4-(2-piperidin-1-ylethoxy)phenyl]methanone according to an analogous synthetic method to Example 337 described below, the total amount of 1-{2-{4-[4-methoxy-2-(7-methoxy-3,4-dihydronaphthalen-2-yl)benzyl]phenoxy}ethyl}piperidine (274 mg) was used according to an analogous synthetic method to Example 30 described below to provide 1-{2-{4-[4-methoxy-2-(7-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)benzyl]phenoxy}ethyl}piperidine (238 mg). This compound (236 mg) was used according to an analogous synthetic method to Example 111 described below to provide the title compound (75 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960412B2
Source datasetuspto-grants-2011_06
ORD IDord-95b99468efbf40fcb4ca0b395f7ea435
Source noteuspto-grants-2011_06