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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352006Generated: October 29, 2026

Triethylamine → HCID 22715005, compound

https://huagongshe.com/reaction/352006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Propanol, 1-amino-2-methyl-HCID 95102—
Reactant2,4-Dichloro-5,6-dimethyl-3-nitropyridineHCID 12109123—
SolventDimethylformamideHCID 6228—
ProductHCID 22715005HCID 22715005—

Reaction Conditions

Temperature5 °C

Reaction Steps

Triethylamine (15.20 ml) was added to a solution of 2,4-dichloro-5,6-dimethyl-3-nitropyridine (16.080 g) in dimethylformamide (160 ml), and then 2-hydroxy-2-methylpropylamine (7.143 g) was added with stirring. After 1 day the resulting mixture was cooled to about 5° C. After 4 days the solvent was removed under reduced pressure, and the resulting oil was dissolved in ethyl acetate (200 ml). The resulting solution was extracted with water (3×65 ml), and the combined aqueous layers were extracted with ethyl acetate (50 ml). The combined organic layers were dried with magnesium sulfate, and the solvent was removed under reduced pressure. The crystals that formed upon cooling were recrystallized from 1:1 hexane/ethyl acetate and then from ethyl acetate. The resulting purified crystals were used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743920B2
Source datasetuspto-grants-2004_06
ORD IDord-35d9dcdf82ba45729414c3feb90cba06
Source noteuspto-grants-2004_06