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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691282Generated: October 27, 2026

Tetramethyltin → Ethyl 2-amino-6-methylnicotinate

https://huagongshe.com/reaction/1691282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethyltinHCID 11661—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantEthyl 2-amino-6-chloronicotinateHCID 45926148—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductEthyl 2-amino-6-methylnicotinateHCID 1249468648%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a N-methylpyrrolidinone (20 mL) solution of 2-amino-6-chloro-nicotinic acid ethyl ester (2.00 g, 7.78 mmol) described in Manufacturing Example 170-1-1 were added tetramethyltin (1.62 mL, 11.7 mmol) and tetrakis(triphenylphosphine)palladium(0) (899 mg, 0.778 mmol), which was stirred under nitrogen atmosphere for 5 hours and 40 minutes at 130° C. Water was added to the reaction mixture at room temperature, which was extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under a reduced pressure. The residue thus obtained was purified by NH silica gel column chromatography (heptane:ethyl acetate=3:1), and then further purified by silica gel column chromatography (heptane:ethyl acetate=2:1) to obtain the title compound (670 mg, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-bdfde941cf904e09871c3797d8c8fc4d
Source noteuspto-grants-2012_04