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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639650Generated: October 26, 2026

Sodium Iodide → (2,6-Dibromo-3-nitro-pyridin-4-yl)-(6-methyl-pyridin-3-ylmethyl)-carbamic acid ethyl ester

https://huagongshe.com/reaction/639650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(Chloromethyl)-2-methylpyridineHCID 12214338—
ReactantEthyl (2,6-dibromo-3-nitropyridin-4-yl)carbamateHCID 86614481—
SolventAcetoneHCID 180—
Product(2,6-Dibromo-3-nitro-pyridin-4-yl)-(6-methyl-pyridin-3-ylmethyl)-carbamic acid ethyl esterHCID 8661448262.3%

Reaction Steps

Potassium carbonate (7.95 g) was added to a stirred solution of (2,6-dibromo-3-nitro-pyridin-4-yl)-carbamic acid ethyl ester (10.62 g) in acetone (100 ml). 5-(chloromethyl)-2-methylpyridine (4.89 g) was then added, followed by sodium iodide (5.18 g). The mixture was left to stir under nitrogen for 18 hours. The reaction mixture was filtered, concentrated in vacuo, and then partitioned between ethyl acetate (100 ml) and water (100 ml). The organics were dried (MgSO4) and evaporated to a dark purple gum, which was columned on Isco Companion on a silica column (330 g, Redisep), eluting with EtOAc:heptane, increasing the gradient linearly from 40:60 to 80:20 over 6 column volumes. This provided the title compound (8.5 g) as a green gum which solidified to a pale green solid on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691877B2
Source datasetuspto-grants-2010_04
ORD IDord-86159069e7824513889a912227c08e04
Source noteuspto-grants-2010_04