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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363994Generated: November 1, 2026

Acetic Acid → Methyl 3-[(1-methylethyl)amino]-5-(pyridin-4-yl)thiophene-2-carboxylate

https://huagongshe.com/reaction/2363994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-MethoxypropeneHCID 8300—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 3-amino-5-(pyridin-4-yl)thiophene-2-carboxylateHCID 43155531—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-[(1-methylethyl)amino]-5-(pyridin-4-yl)thiophene-2-carboxylateHCID 6674384946.3%

Reaction Steps

To a mixture of methyl 3-amino-5-(pyridin-4-yl)thiophene-2-carboxylate (0.469 g, 2.00 mmol), 2-methoxypropene (0.29 mL, 3.0 mmol) and acetic acid (0.114 mL, 2.00 mmol) in dichloromethane (6 mL) was added sodium triacetoxyborohydride (0.636 g, 3.00 mmol), and the reaction was stirred at room temperature overnight. Then, the reaction mixture was poured into sat. NaHCO3 (70 mL) and extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with brine (50 mL), dried over magnesium sulfate, filtered, and concentrated, and the residue was purified by flash chromatography (Combiflash, silica gel, hexanes to ethyl acetate) to give the title compound (0.256 g, 46%) as a yellow solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691828B2
Source datasetuspto-grants-2014_04
ORD IDord-2525a4f7f4244a4ab432b7f44f8b08fa
Source noteuspto-grants-2014_04