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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667429Generated: October 31, 2026

Binap, (A+-)- → HCID 58447358, compound

https://huagongshe.com/reaction/1667429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
Reactant[2-(2-morpholinoethoxy)phenyl]methylamineHCID 7537544—
ReactantSodium t-butoxideHCID 23676156—
Reactant6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 58447358HCID 58447358—

Reaction Steps

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (70 mg, 0.27 mmol), 2-(2-morpholin-4-yl-ethoxy)-benzylamine (83 mg, 0.35 mmol), Pd2(dba)3 (25 mg, 0.027 mmol), rac-BINAP (51 mg, 0.081 mmol) and NaOt-Bu (76 mg, 0.81 mmol) in DMA (6 mL) was heated at 80° C. for 1 h. The mixture was allowed to cool, diluted with EtOAc (25 mL) and washed with water (25 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated. Chromatography on silica (EtOAc/hexanes) yielded the title compound. 4-Chloro-6-[2-(2-morpholin-4-yl-ethoxy)-benzylamino]-2H-phthalazin-1-one: 28 mg (25.0%): m/z (M+H)=415. 1H-NMR (DMSO-d6) δ: 12.33 (s, 1H), 7.91 (d, 1H), 7.45 (m, 1H), 7.24 (m, 2H), 7.13 (m, 1H), 7.04 (m, 1H), 6.90 (m, 1H), 6.79 (s, 1H), 4.36 (d, 2H), 4.15 (t, 2H), 3.51 (t, 4H), 2.72 (t, 2H), 2.45 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044041B2
Source datasetuspto-grants-2011_10
ORD IDord-c4d4efa0481d4300a78ee60077296f0e
Source noteuspto-grants-2011_10