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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16010Generated: October 28, 2026

Dichloromethane → HCID 59341976, compound

https://huagongshe.com/reaction/16010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinolineHCID 54775608—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
SolventDimethylacetamideHCID 31374—
ProductHCID 59341976HCID 5934197688%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a suspension of 6-[(6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl]quinoline (1.0 g, 2.93 mmol) in DMAC (70 ml) were added zinc cyanide (413 mg, 3.52 mmol). The reaction mixture was degassed then PdCl2(dppf).CH2Cl2 (240 mg, 0.29 mmol) was added followed with triethylamine (0.828 ml) at R.T. The reaction mixture was degassed again. After heating at 85° C., the reaction mixture was filtered through a celite pad and washed with 5.0 ml of CH2Cl2. The solvents were concentrated under reduced pressure. The resulting residue was purified via flash column chromatography eluted with 1-3% 7N N3 in MeOH:CH2Cl2 to give the desired product (740 mg, 88%). 1H NMR (400 MHz, DMSO-d6) δ ppm 6.28 (s, 2H) 7.55 (dd, J=8.34, 4.29 Hz, 1H) 7.81 (dd, J=8.72, 2.15 Hz, 1H) 7.99-8.04 (m, 2H) 8.33-8.37 (m, 1H) 8.91 (dd, J=4.04, 1.77 Hz, 1H) 9.41 (s, 1H) APCI (Mz+1) 288.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732604B2
Source datasetuspto-grants-2010_06
ORD IDord-205a032962f04956924f59a8bddc024b
Source noteuspto-grants-2010_06