HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333557Generated: October 30, 2026
3-Iodo-N-methylpyridin-2-amine → HCID 68205837, compound
https://huagongshe.com/reaction/333557
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Iodo-N-methylpyridin-2-amine | HCID 14047146 | — |
| Reactant | HCID 21735431 | HCID 21735431 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Catalyst | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68205837 | HCID 68205837 | 91% |
Reaction Steps
A 1 L round-bottomed flask was charged with 3-iodo-N-methylpyridin-2-amine (8.95 g, 38.3 mmol), N1,N1-diphenylbenzene-1,3-diamine (9.96 g, 38.3 mmol), dicyclohexyl(2′,4′,6′-triisopropyl-[1,1′-biphenyl]-2-yl)phosphine (0.183 g, 0.384 mmol) and sodium 2-methylpropan-2-olate (5.15 g, 53.6 mmol) in toluene (500 mL). Nitrogen was bubbled through for 10 minutes. Then Pd2 dba3 (88 mg, 0.10 mmol) was added and this was stirred at 120° C. for overnight. The mixture was then filtered and the filtrate was concentrated and chromatographed using a mobile phase gradient of 0-20% ethyl acetate in dichloromethane to give N3-(3-(diphenylamino)phenyl)-N2-methylpyridine-2,3-diamine (12.2 g, 91% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883322B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-828736f310194f469037dceba4446170 |
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| Source note | uspto-grants-2014_11 |
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