HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882249Generated: October 30, 2026
2-Amino-3-bromo-5-methylpyridine → HCID 58880142, compound
https://huagongshe.com/reaction/1882249
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Amino-3-bromo-5-methylpyridine | HCID 519380 | — |
| Reactant | 4-Chloro-2-iodoanisole | HCID 2800978 | — |
| Catalyst | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 58880142 | HCID 58880142 | 84.3% |
Reaction Steps
In a oven dried 50 mL round bottom flask were sequentially added 4-chloro-2-iodo-1-methoxybenzen (1.13 g, 4.2 mmol), 3-bromo-5-methylpyridin-2-amine (945 mg, 5.05 mmol), Pd2(dba)3 (192 mg, 0.21 mmol), xantphos (146 mg, 0.06 mmol) and NatBuO (605 mg, 6.3 mmol) at room temperature. The solid materials were kept under vacuum for 5 min. and then refilled with nitrogen. This process was repeated thrice before adding dry, degassed dioxane (10 mL). The heterogeneous mixture was stirred at room temperature for 15 min. and then at 100° C. for 1 h. Finally upon completion of the reaction, it was diluted with ether and filtered through a small pad of silica gel with several washings. All the washings and filtrate concentrated in vacuum and the crude residue was further purified by flash chromatography to provide title compound (1.16 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318939B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-082c8a862fee4a7ea33ef0baa187207d |
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| Source note | uspto-grants-2012_11 |
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