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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424205Generated: November 1, 2026

HCID 2994469, compound → HCID 23087116, compound

https://huagongshe.com/reaction/2424205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 2994469HCID 2994469—
ReactantHCID 14425930HCID 14425930—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 23087537HCID 23087537—
ProductHCID 23087116HCID 23087116—

Reaction Steps

Obtained by reducing 4-(2-piperidin-1-ylethoxy)benzonitrile with lithium aluminum hydride, 4-(2-piperidin-1-ylethoxy)benzylamine (1.3 g) and 2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-ylmethyl)phenyl trifluoromethanesulfonate (1.4 g) were used according to an analogous synthetic method to Example 116 to provide [2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-ylmethyl)phenyl][4-(2-piperidin-1-ylethoxy)benzyl]amine (1.2 g). A portion thereof (200 mg) was used according to an analogous synthetic method to Example 364 to provide the title compound (100 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960412B2
Source datasetuspto-grants-2011_06
ORD IDord-6f4da8ce3f39402b9416026c3113c5fb
Source noteuspto-grants-2011_06