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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544838Generated: October 31, 2026

2-Chloro-5-nitropyrimidine → HCID 66631372, compound

https://huagongshe.com/reaction/544838

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitropyrimidineHCID 82544—
Reactant1,4-Diazabicyclo(3.2.2)nonaneHCID 398407—
ReactantSodium BicarbonateHCID 516892—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 66631372HCID 66631372—

Reaction Steps

A mixture of 1,4-diazabicyclo[3.2.2]nonane (0.87 g, 6.90 mmol), 2-chloro-5-nitro-pyrimidine (1.56 g, 6.27 mmol) and dioxane (75 ml) was stirred at room-temperature for 15 h. Aqueous sodium bicarbonate (20 ml, 10%) was added followed by extraction with ethylacetate (3×20 ml). The organic phase was dried and evaporated and a yellow powder was isolated. Yield 0.86 g (55%). Mp 135-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935695B2
Source datasetuspto-grants-2011_05
ORD IDord-db179f7c42db4ba0b5e0c3cd9209b495
Source noteuspto-grants-2011_05