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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056739Generated: October 26, 2026

Binap, (A+-)- → (3R)-3-methyl-1-(1H,3H-naphtho[1,8-cd]pyran-6-yl)piperazine

https://huagongshe.com/reaction/2056739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
Reactant2-Methylpiperazine, (R)-HCID 7330434—
ReactantSodium t-butoxideHCID 23676156—
Reactant6-bromo-1H,3H-naphtho[1,8-cd]pyranHCID 69307283—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product(3R)-3-methyl-1-(1H,3H-naphtho[1,8-cd]pyran-6-yl)piperazineHCID 69306502—

Reaction Steps

A mixture of 6-bromo-1H,3H-naphtho[1,8-cd]pyran (0.30 g, 1.2 mmol), 2-(R)-methylpiperazine (0.145 g, 1.44 mmol), tris(dibenzylideneacetone)dipalladium(0) (55 mg, 0.06 mmol), rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (56 mg, 0.09 mmol) and sodium tert-butoxide (0.162 g, 1.68 mmol) in toluene (5 mL) was heated under reflux for 2 h. The solvent was evaporated in vacuo and the crude mixture purified by column chromatography on silica gel, eluting with dichloromethane/methanol (9:1), to yield (3R)-3-methyl-1-(1H,3H-naphtho[1,8-cd]pyran-6-yl)piperazine as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335660B2
Source datasetuspto-grants-2008_02
ORD IDord-3246601d97494adcb52ff263b8e80177
Source noteuspto-grants-2008_02