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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173066Generated: November 2, 2026

Binap, (A+-)- → HCID 67367138, compound

https://huagongshe.com/reaction/1173066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
Reactant(2R)-2-(Methoxymethyl)pyrrolidineHCID 671216—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 67365915HCID 67365915—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67367138HCID 6736713818%

Reaction Steps

A solution of 0.07 g rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (BINAP, 0.11 mmol) and 0.043 g tri(dibenzylideneacetone)dipalladioum(0) (0.05 mmol) in 5 ml tetrahydrofuran were added dropwise to a solution of 4-bromo-N-[4-((1R,5S,6R)-3-propyl-3-aza-bicyclo[3.2.0]hept-6-yl)-phenyl]-benzenesulfonamide (0.26 g, 0.59 mmol), (R)-2-(methoxymethyl)pyrrolidine (104 mg, 0.9 mmol), and 0.104 g sodium tert.butylate (1.08 mmol) in 20 ml tetrahydrofuran. The reaction mixture was refluxed for 5½ hours, and, after additional addition of 0.04 ml (R)-2-(methoxymethyl)pyrrolidine, for another 2 hours. After evaporation, the residue was treated with water, extracted twice with diethyl ether and dichloromethane each, and the combined organic layers dried over magnesium sulfate, filtered, and the solvent evaporated. Purification of the thus obtained crude product via silica gel chromatography using a gradient of dichloromethane/methanol 0-12% gave 50 mg (yield 18%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834048B2
Source datasetuspto-grants-2010_11
ORD IDord-265b458b303c40ed885ba9b763267353
Source noteuspto-grants-2010_11