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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47883Generated: October 26, 2026

Sodium Iodide → 5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/47883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantHCID 178438045HCID 178438045—
SolventWaterHCID 962—
SolventMethyl Ethyl KetoneHCID 6569—
Product5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamideHCID 1121871774%

Reaction Steps

A mixture of 3-ethyl-4-nitro-1H-pyrazole-5-carboxamide (25 g, 0.136 Mol), sodium carbonate (18 g, 0.17 Mol) and sodium iodide (20.4 g, 0.136 Mol) were suspended in ethyl methyl ketone (125 mL) at room temperature. 2-bromoethyl methyl ether (12.8 mL, 0.142 Mol) was added and the mixture was heated to reflux and stirred for 70 hours. The mixture was cooled to ambient temperature and water (250 mL) was added. The resultant slurry was warmed to reflux and held at that temperature for 30 min before cooling to room temperature. The resultant precipitate was granulated at room temperature for 3 h, filtered and vacuum dried to afford 5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamide as a yellow crystalline solid 24.3 g, 74%. Data as reported for Example (g)(i).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699991B2
Source datasetuspto-grants-2004_03
ORD IDord-3b5f06b838194b6a9ad7bbc738c90123
Source noteuspto-grants-2004_03