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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416857Generated: November 1, 2026

Sodium Dithionite → HCID 178488879, compound

https://huagongshe.com/reaction/416857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
Reactant4-MethoxybenzaldehydeHCID 31244—
Reactant5-Bromo-3-nitro-4-(4-(pyrimidin-5-ylmethyl)piperazin-1-yl)pyridin-2-amineHCID 46868780—
ReactantHCID 178482685HCID 178482685—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 178488879HCID 17848887952%

Reaction Steps

This was prepared using the same procedure as for 4-(6-bromo-2-(4-(dimethylamino)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)-N-phenylpiperazine-1-carboxamide, but here using 5-bromo-3-nitro-4-(4-(pyrimidin-5-ylmethyl)piperazin-1-yl)pyridin-2-amine (30 mg, 0.076 mmol), DMF (0.15 mL), ethanol (0.85 mL), 1M Na2S2O4 (3 eq, 0.23 mmol, 0.23 mL) and 4-methoxybenzene carboxaldehyde (1.1 eq, 0.083 mmol, 12 mg). After 6 h, concentration in vacuo and purification by preparative tlc (CH2Cl2-MeOH, 95:5) gave the product (19 mg, 52%) as a colourless solid; δH (500 MHz, DMSO-d6) 2.64 (s, br, 4H, piperazine N(CH2)2), 3.64 (s, 2H, NCH2), 3.66 (t, J=4.6 Hz, 4H, piperazine N(CH2)2), 3.84 (s, 3H, OCH3), 7.09 (d, J=8.9 Hz, 2H, methoxyphenyl H-2 & H-6), 8.13 (d, J=8.9 Hz, 2H, methoxyphenyl H-3 & H-5), 8.20 (s, 1H, imidazo[4,5-b]pyridine H-5), 8.80 (s, 2H, pyrimidine H-4 & H-6), 9.12 (s, 1H, pyrimidine H-2), 13.35 (s, br, 1H, imidazo[4,5-b]pyridine NH);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088761B2
Source datasetuspto-grants-2012_01
ORD IDord-d089f03d819848479c84073d3f4be7e8
Source noteuspto-grants-2012_01