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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522376Generated: November 3, 2026

1,2-Dichloroethane → HCID 41507106, compound

https://huagongshe.com/reaction/1522376

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylmorpholineHCID 7972—
ReactantHOAtHCID 181649—
Reactant6-phenyl-1-(propan-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acidHCID 2535053—
Reactant3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridin-2-oneHCID 7063844—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 41507106HCID 4150710670%

Reaction Steps

In a 25 mL sealable tube under nitrogen were combined 1-(1-methylethyl)-6-phenyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (70 mg, 0.25 mmol) and 3-(aminomethyl)-4,6-dimethyl-2(1H)-pyridinone.HCl (56.3 mg, 0.3 mmol) in DMSO (3 mL). 1-hydroxy-7-azabenzotriazole (51 mg, 0.37 mmol) was added and the resulting mixture was degassed with nitrogen for 10 min. N-methylmorpholine (0.1 ml, 0.87 mmol) and EDC (72 mg, 0.37 mmol) were added, the vessel was sealed, and the bright yellow mixture was stirred at room temperature for 2 days. Next added 2 mL of water, and the contents were stirred for 10 min. Solids that precipitated were sonicated, and allowed to stand at room temperature for 10 min. The reaction contents were filtered and washed with water. The solid was treated with 2 mL of EtOH, sonicated and heated, and then allowed to cool to room temperature. The contents were filtered, washed with water and dried to afford the title compound (74 mg, 70%) as a white solid. LCMS E-S (M+H)=416.3. 1H NMR (400 MHz, DMSO-d6) δ ppm 11.58 (s, 1 H), 8.98 (t, J=4.80 Hz, 1 H), 8.38 (s, 1 H), 8.25-8.30 (m, 2 H), 8.17 (s, 1 H), 7.49-7.59 (m, 3 H), 5.91 (s, 1 H), 5.30-5.38 (m, 1 H), 4.42 (d, J=4.80 Hz, 2 H), 2.23 (s, 3 H), 2.13 (s, 3 H), 1.55 (d, J=6.57 Hz, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073924B2
Source datasetuspto-grants-2015_07
ORD IDord-603b184fa1f64ceab7f16f221c2e6145
Source noteuspto-grants-2015_07