HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966235Generated: October 30, 2026
1-Methyl-3-aminopyrazole → HCID 25261183, compound
https://huagongshe.com/reaction/1966235
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methyl-3-aminopyrazole | HCID 137254 | — |
| Reactant | HCID 86644606 | HCID 86644606 | — |
| Catalyst | HCID 178482626 | HCID 178482626 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 25261183 | HCID 25261183 | 55% |
Reaction Steps
2-Bromo-5-(4-methanesulfonyl-phenoxy)-pyridine (0.47 mmol), sodium-tert.-butylate (1.4 eq.), and 1-methyl-1H-pyrazole-3-amine (1.2 eq.) are dissolved in degassed dioxane (2.5 ml) and heated to 80° C. Chloro(di-2-norbornylphosphino)(2-dimethylaminoferrocene-1-yl)palladium (II) (5.9 mg) in degassed dioxane (1 ml) is added and the reaction mixture is heated for 1 hour at 142° C. in the microwave. The reaction is quenched with ethylacetate (30 ml) and filtrated over celite. The solvent of the filtrate is removed in vacuo [5-(4-Methanesulfonyl-phenoxy)-pyridine-2-yl]-(1-methyl-1H-pyrazole-3-yl)-amine (“A27”) is obtained after reversed phase column chromatography (water/acetonitrile+0.1% TFA) as orange powder in a yield of 55%; HPLC (method C): 1.57 min; LC-MS (method A): 0.787 min, 345.15 (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-0745bec8d1cb4998af06f4655b906f46 |
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| Source note | uspto-grants-2013_04 |
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