Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667484Generated: October 30, 2026

2-Pyridinemethanamine → HCID 24948339, compound

https://huagongshe.com/reaction/1667484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyridinemethanamineHCID 19509—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Reactant6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 24948339HCID 249483391.8%

Reaction Steps

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (153 mg, 0.590 mmol), 2-(aminomethyl)pyridine (0.066 mL, 0.646 mmol), Pd2(dba)3 (49 mg, 0.0535 mmol), rac-BINAP (113 mg, 0.181 mmol) and NaOtBu (160 mg, 1.665 mmol) in DMA (5 mL) was heated at 85° C. for 1.5 h. The mixture was allowed to cool, diluted with EtOAc and washed with water. The organic layer was washed with sat.aq. NaHCO3, brine and dried (Na2SO4). Chromatography on silica (EtOAc/hexanes) afforded 4-chloro-6-[(pyridin-2-ylmethyl)-amino]-2H-phthalazin-1-one (3 mg) as a yellow brown solid, 1H (400 MHz, d6-DMSO) δ: 4.53 (d, 2H), 6.84 (s, 1H), 7.18 (dd, 1H), 7.28 (m, 1H), 7.38 (d, 1H), 7.75 2H), 7.92 (d, 1H), 8.55 (d, 1H), 12.35 (s, 1H) ppm; m/z (M+1) 286.99.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044041B2
Source datasetuspto-grants-2011_10
ORD IDord-2173d13a88e74812bab3f88bb810e301
Source noteuspto-grants-2011_10