HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668968Generated: October 31, 2026
Phosphorus oxychloride → 3-Bromo-7-chloro-2-methylthieno[2,3-c]pyridine
https://huagongshe.com/reaction/1668968
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3-bromo-2-methylthieno[2,3-c]pyridine-N-Oxide | HCID 67339746 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Bromo-7-chloro-2-methylthieno[2,3-c]pyridine | HCID 58466457 | — |
Reaction Steps
3-Bromo-2-methylthieno[2,3-c]pyridine-N-Oxide (0.500 g, 2.05 mmol) was dissolved in chloroform (10 mL) and treated with phosphorous oxychloride (0.955 ml, 10.2 mmol). The reaction was heated to 70° C. while stirring. After 3 hours, the volatiles were removed in vacuo and the residual phosphorous oxychloride was azeotroped with toluene. The resulting residue was taken up in DCM and washed (2×) with an aqueous saturated solution of sodium bicarbonate, then with water and then brine. The organic layer was then dried with sodium sulfate and purified by column chromatography on silica gel using a gradient of 20-60% EtOAc in hexanes to give 3-bromo-7-chloro-2-methylthieno[2,3-c]pyridine as a yellow solid. MS (M+H)+ 263.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989461B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-904f2d12124047e0becc5206b44233b4 |
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| Source note | uspto-grants-2011_08 |
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