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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416882Generated: October 25, 2026

1-Ethylpiperazine → 5-Chloro-4-(4-ethylpiperazin-1-yl)-3-nitropyridin-2-amine

https://huagongshe.com/reaction/416882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-EthylpiperazineHCID 79196—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-4,5-dichloro-3-nitropyridineHCID 46867660—
Reactant2-(4-(2-amino-5-bromo-3-nitropyridin-4-yl)piperazin-1-yl)-N-(thiazol-2-yl)acetamideHCID 46867803—
SolventIsopropanolHCID 3776—
Product5-Chloro-4-(4-ethylpiperazin-1-yl)-3-nitropyridin-2-amineHCID 5789715331%

Reaction Steps

This was prepared using the same procedure as for 2-(4-(2-amino-5-bromo-3-nitropyridin-4-yl)piperazin-1-yl)-N-(thiazol-2-yl)acetamide, but here using 4,5-dichloro-3-nitropyridin-2-amine (75 mg, 0.36 mmol), iPrOH (2 mL), DIPEA (3.5 eq, 1.26 mmol, 0.22 mL) and 1-ethylpiperazine (1.2 eq, 0.43 mmol, 0.05 mL). Concentration in vacuo and purification by preparative tlc (CH2Cl2-MeOH, 95:5) gave the product (32 mg, 31%) as a yellow solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088761B2
Source datasetuspto-grants-2012_01
ORD IDord-6d8ce21d3d684d39bd7600be43ef4a93
Source noteuspto-grants-2012_01