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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356250Generated: October 27, 2026

N2-Methyl-5-(trifluoromethyl)pyridine-2,3-diamine → HCID 10670561, compound

https://huagongshe.com/reaction/356250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN2-Methyl-5-(trifluoromethyl)pyridine-2,3-diamineHCID 2735930—
Reactant5-[4-(2-Oxoethoxy)benzyl]thiazolidine-2,4-dioneHCID 10849277—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 10670561HCID 106705617.6%

Reaction Steps

4.16 g of 5-(4-(2-oxoethoxy)benzyl)thiazolidine-2,4-dione (prepared as described in Preparation 47) were added to a solution of 3.00 g of 3-amino-2-methylamino-5-trifluoromethylpyridine in a mixture of 6 ml of ethanol and 6 ml of acetic acid, and the resulting mixture was stirred at room temperature for 4 hours. At the end of this time, the reaction mixture was freed from the solvent by distillation under reduced pressure. 50 ml of 1,2-dimethoxyethane and 5.2 g of iodine were added to the residue, and the resulting mixture was stirred at 60° C. for one day. At the end of this time, the reaction mixture was poured into water, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate, after which the solvent-was removed by distillation under reduced pressure. The residue was purified by column chromatography through silica gel, using a 1:1 by volume mixture of hexane and ethyl acetate as the eluent. The product was crystallized by trituration with ethyl acetate, to give 520 mg of the title compound, melting at 212°-214° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834501
Source datasetuspto-grants-1998_11
ORD IDord-e1bd5de54f2142feaa60c8ddc29e1c73
Source noteuspto-grants-1998_11