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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ethyl 4-amino-6-methylthieno[2,3-b]pyridine-5-carboxylate | HCID 68323805 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl 4-amino-2-bromo-6-methylthieno[2,3-b]pyridine-5-carboxylate | HCID 68323734 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029545B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-e6c1134a44e6478ca606237198ff9971 |
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| Source note | uspto-grants-2015_05 |
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