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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255434Generated: November 1, 2026

Hydrochloric Acid → 5-Ethyl 3-methyl 6-(difluoromethyl)-4-(isopropylamino)-2-(trifluoromethyl)-3,5-pyridinedicarboxylate

https://huagongshe.com/reaction/255434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
ReactantDimethyl 6-(difluoromethyl)-4-(iso propylamino)-2-(trifluoromethyl)-3,5-pyridine-dicarboxylateHCID 14013774—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Ethyl 3-methyl 6-(difluoromethyl)-4-(isopropylamino)-2-(trifluoromethyl)-3,5-pyridinedicarboxylateHCID 14013820775.4%

Reaction Steps

A mixture of 4.1 g (0.001 mol) of product of Example 76, 0.62 g (0.011 mol) of KOH and 5 ml of H2O overnight. The reaction mixture was poured into 250 ml of H2O containing 50 ml of concentrated HCl, extracted with ether, dried (mgSO4) and concentrated in vacuo to 3.76 g of yellow air. This oil, 152 g (0.011 mol) of K2CO3 and 0.88 ml (0.011 mol) of ethyl iodide in 30 ml of DMF was stirred at room temperature overnight. The reaction mixture was poured into water extracted with ether, drid (MgSO4) and concentrated in vacuo to 3.64 g of yellow oil. Kugelrohr distillation at 53 Pa, pot temperature 103° C., afforded 2.98 g (70.5%) of product sa a light yellow oil which solidified; mp 37°-39° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698093
Source datasetuspto-grants-1987_10
ORD IDord-4c69d8c06b17479a8ddebe5a4d38deab
Source noteuspto-grants-1987_10