HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966230Generated: October 31, 2026
1-Methyl-3-aminopyrazole → HCID 25261180, compound
https://huagongshe.com/reaction/1966230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methyl-3-aminopyrazole | HCID 137254 | — |
| Reactant | 2-Bromo-5-methoxypyridine | HCID 11148151 | — |
| Catalyst | HCID 178482626 | HCID 178482626 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 25261180 | HCID 25261180 | 55% |
Reaction Steps
2-Bromo-5-methoxy-pyridine (0.97 mmol), sodium-tert.-butylate (1.5 eq.), and 1-methyl-1H-pyrazole-3-amine (1.3 eq.) are dissolved in degassed dioxane (2 ml) and heated to 80° C. Chloro-(di-2-norbornylphosphino)(2-dimethylaminoferrocene-1-yl)palladium (II) (5 mg) in degassed dioxane (1 ml) is added and the reaction is heated for 20 hours at 110° C. The reaction is quenched with ethylacetate/methanol (30 ml, 9:1) and filtrated over celite. The solvent of the filtrate is removed in vacuo. (5-Methoxy-pyridine-2-yl)-(1-methyl-1H-pyrazole-3-yl)-amine (“A24”) is obtained after reversed phase column chromatography (water/acetonitrile+0.1% TFA) as colorless powder in a yield of 55%; HPLC (method C): 1.09 min; LC-MS (method A): 0.73 min, 205.0 (M+H+);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420642B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-a4f15915cb50453781233f67e39f75e1 |
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| Source note | uspto-grants-2013_04 |
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