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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-(Chloromethyl)-2-methylpyridine | HCID 12214338 | — |
| Reactant | Ethyl (2,6-dibromo-3-nitropyridin-4-yl)carbamate | HCID 86614481 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (2,6-Dibromo-3-nitro-pyridin-4-yl)-(6-methyl-pyridin-3-ylmethyl)-carbamic acid ethyl ester | HCID 86614482 | 62.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691877B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-86159069e7824513889a912227c08e04 |
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| Source note | uspto-grants-2010_04 |
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