反应 #385

ord-067f9706b99f4ac98e07f49d63946447

反应方程式

Cc1cc(Nc2cc(I)c(C(F)(F)F)cn2)n(C)n1
Cc1cc(Nc2cc(I)c(C(F)
CONC(=O)c1c(N)cccc1OC
CONC(=O)c1c(N)cccc1O
CONC(=O)c1c(Nc2cc(Nc3cc(C)nn3C)ncc2C(F)(F)F)cccc1OC
CONC(=O)c1c(Nc2cc(Nc

溶剂

反应条件

温度
90°CELSIUS

实验过程

N-(1,3-dimethyl-1H-pyrazol-5-yl)-4-iodo-5-(trifluoromethyl)pyridin-2-amine (50 mg, 0.13 mmol), 2-amino-N,6-dimethoxybenzamide (43.6 mg, 0.22 mmol), diacetoxypalladium (1.469 mg, 6.54 µmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (7.57 mg, 0.01 mmol) and potassium carbonate (36.2 mg, 0.26 mmol) were suspended in 1,4-dioxane (423 µl) and sealed into a microwave tube. The reaction was degased, purged with nitrogen and heated to 90 °C overnight => _not complete but seemed to be clean, no des-iodo by-product formed, both SM left_ Same reaction was performed in toluene (423 µl) => _reaction complete, LCMS profile similar to the conception document reference_ **_NOT ISOLATED_**

来源

750 AstraZeneca ELN dataset