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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522460Generated: October 31, 2026

1,2-Dichloroethane → HCID 56598944, compound

https://huagongshe.com/reaction/1522460

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
ReactantHOAtHCID 181649—
Reactant3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridin-2-oneHCID 7063844—
ReactantHCID 16792462HCID 16792462—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 56598944HCID 56598944—

Reaction Steps

The title compound was prepared in the same manner as described for intermediate 56 using 6-cyclopropyl-1-(2-methylpropyl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (80 mg, 0.309 mmol), 3-(aminomethyl)-4,6-dimethyl-2(1H)-pyridinone (70.4 mg, 0.463 mmol), 1-hydroxy-7-azabenzotriazole (84 mg, 0.617 mmol), DMSO(10 mL), EDC (118 mg, 0.617 mmol), and N-methylmorpholine (0.136 mL, 1.234 mmol). The final product was collected as 0.123 g (100%). LCMS E-S (M+H)=394.2 1H NMR (400 MHz, DMSO-d6) δ ppm 0.93-1.12 (m, 4 H), 1.42 (d, J=6.82 Hz, 6 H), 2.12 (s, 3 H), 2.22 (s, 4 H), 2.36 (s, 3 H), 4.34 (d, J=4.80 Hz, 2 H), 4.90-5.11 (m, 1 H), 5.87 (s, 1 H), 6.99 (s, 1 H), 8.58 (s, 1 H), 11.51 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073924B2
Source datasetuspto-grants-2015_07
ORD IDord-4d90ab3200f040a1a72b26f2d6af57ca
Source noteuspto-grants-2015_07