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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852700Generated: November 3, 2026

Tert-butyl (2,6-dichloro-3-nitropyridin-4-yl)carbamate → Tert-butyl (3-amino-2,6-dichloropyridin-4-yl)carbamate

https://huagongshe.com/reaction/1852700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl (2,6-dichloro-3-nitropyridin-4-yl)carbamateHCID 86671448—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductTert-butyl (3-amino-2,6-dichloropyridin-4-yl)carbamateHCID 86724467—

Reaction Steps

A mixture of tert-butyl (2,6-dichloro-3-nitropyridin-4-yl)carbamate (700 g, 2.27 mol) and iron (1272.7 g, 22.7 mol) in ethanol (5 L) and water (1 L) was stirred at room temperature for 10 h. The mixture was filtered, the filtrate was concentrated in vacuo, and the crude product was crystallized using EtOAc to give tert-butyl (3-amino-2,6-dichloropyridin-4-yl)carbamate. Preparative Example 2.3 4,6-dichloro-3-((trans-4-methylcyclohexyl)methyl)-3H-imidazo[4,5-c]pyridine

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962611B2
Source datasetuspto-grants-2015_02
ORD IDord-4a9398b46ba04675b3cf0a4b4d405000
Source noteuspto-grants-2015_02