HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774763Generated: November 1, 2026
3-Bromo-5-iodopyridine → HCID 86679137, compound
https://huagongshe.com/reaction/1774763
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Bromo-5-iodopyridine | HCID 820409 | — |
| Reactant | HCID 86280124 | HCID 86280124 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86679137 | HCID 86679137 | 58.4% |
Reaction Steps
To a solution of 3-bromo-5-iodopyridine (0.14 g, 0.493 mmol) in THF (2 mL) cooled at −78° C. was added nBuLi (462 μl, 0.74 mmol) dropwise over 5 min. The reaction mixture was stirred at −78° C. for 15 min, then (R)-2-methyl-N-(oxetan-3-ylidene)-propane-2-sulfinamide (0.1 g, 0.567 mmol) in THF (1 mL) was added dropwise. The reaction mixture was stirred at −78° C. for 10 min then allowed to warm up to RT. The mixture was quenched with water (2 mL) and extracted with EtOAc (2×10 mL). Combined organics were dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by silica gel flash chromatography eluting with a 0 to 100% EtOAc-heptane gradient to give the title compound (0.096 g, 58%) as a light yellow oil. MS: 333.0 and 335.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260408B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-25092a209d824649be2e3f0e0b3e12b0 |
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| Source note | uspto-grants-2016_02 |
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