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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658153Generated: October 27, 2026

Methyl 3-aminothieno[3,2-b]pyridine-2-carboxylate → Methyl thieno(3,2-b)pyridine-2-carboxylate

https://huagongshe.com/reaction/658153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-aminothieno[3,2-b]pyridine-2-carboxylateHCID 13793447—
ReactantSodium NitriteHCID 23668193—
ProductMethyl thieno(3,2-b)pyridine-2-carboxylateHCID 22047416—

Reaction Steps

The synthesis is carried out according to the general procedure; for work-up, the resulting precipitate is filtered off with suction and washed repeatedly with water, ethyl acetate and THF. The organic phases of the resulting filtrates are separated off, the aqueous phase is washed with ethyl acetate and the combined organic phases are dried and concentrated. The resulting product is purified by preparative HPLC. Using 2.40 g (11.53 mmol) of methyl 3-aminothieno[3,2-b]pyridine-2-carboxylate and 2.54 g (36.88 mmol) of sodium nitrite, 0.12 g (5% of theory) of the desired product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076355B2
Source datasetuspto-grants-2011_12
ORD IDord-6a0cc1f90e2548659bf8931fdf6e1dc2
Source noteuspto-grants-2011_12