HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62502Generated: October 30, 2026
Potassium Phosphate, Tribasic → 2-[(2,5-dichloro-4-pyridinyl)amino]-N-(methyloxy)benzamide
https://huagongshe.com/reaction/62502
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Amino-N-methoxybenzamide | HCID 12392707 | — |
| Reactant | 2,5-Dichloro-4-iodopyridine | HCID 53400965 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Bis[2-(diphenylphosphino)phenyl] ether | HCID 4285986 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-[(2,5-dichloro-4-pyridinyl)amino]-N-(methyloxy)benzamide | HCID 57516896 | 87.5% |
Reaction Steps
A mixture of 2,5-dichloro-4-iodo-pyridine (40 g, 146.5 mmole, 1 eq), 2-amino-N-methoxy-benzamide (24.32 g, 146.5 mmole, 1 eq) and K3PO4 (77.72 g 366.2 mmole, 2.5 eq) in 1,4-dioxane (600 mL) was degassed with N2 for 1 h. To this were added Pd(OAc)2 (0.657 g, 2.93 mmole, 0.02 eq), DPEPhos (6.31 g, 11.7 mmole, 0.08 eq) and again degassed for 15 min with N2. The resulting mixture was stirred at 110° C. for overnight. After completion of reaction, solid material was collected by filtration, dissolved in water (500 mL) and extracted with ethyl acetate (5×200 mL). Combined organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure. Solid compound so obtained was purified by washing with hexane to give the title compound as yellowish solid (40 g, 53%). 1H-NMR (400 MHz, DMSO-d6): δ 3.63 (s, 3H), 7.06 (s, 1H), 7.15-7.22 (m, 1H), 7.48-7.57 (m, 2H), 7.66-7.67 (d, 1H, J=7.48 Hz), 8.25 (s, 1H), 10.66-11.45 (brs, 1H). LC-MS [M+H]+=312.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09446034B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-c9e09b0554cb4812a5d43ba4fb268a88 |
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| Source note | uspto-grants-2016_09 |
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