Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573586Generated: October 30, 2026

Bromine → Ethyl 4-amino-2-bromo-6-methylthieno[2,3-b]pyridine-5-carboxylate

https://huagongshe.com/reaction/573586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantEthyl 4-amino-6-methylthieno[2,3-b]pyridine-5-carboxylateHCID 68323805—
SolventAcetic AcidHCID 176—
ProductEthyl 4-amino-2-bromo-6-methylthieno[2,3-b]pyridine-5-carboxylateHCID 6832373487%

Reaction Steps

To a stirred solution of ethyl 4-amino-6-methylthieno[2,3-b]pyridine-5-carboxylate (Description 65) (1 g, 4.23 mmol) in acetic acid (3 mL) was added bromine (0.65 mL, 12.70 mmol) and the resulting mixture stirred at RT overnight (ca. 18 h). The reaction was quenched by pouring the reaction mixture into water and the aqueous solution was basified with NaOH (5M) and diluted with ethyl acetate (30 mL). The organic layer was separated and the aqueous layer was re-extracted with ethyl acetate (20 mL×3). The combined organics were washed with saturated sodium thiosulphate solution, dried and concentrated. Purification by chromatography on silica, eluting with a gradient of 0-30% ethyl acetate in DCM afforded the title compound (1.16 g). LCMS (A) m/z: 315/317 [M+1]+, Rt 0.95 min (acidic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029545B2
Source datasetuspto-grants-2015_05
ORD IDord-e6c1134a44e6478ca606237198ff9971
Source noteuspto-grants-2015_05