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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110182Generated: October 30, 2026

Methyl iodide → HCID 58763656, compound

https://huagongshe.com/reaction/2110182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
ReactantHCID 58763637HCID 58763637—
SolventDimethylformamideHCID 6228—
ProductHCID 58763651HCID 5876365119%
ProductHCID 58763656HCID 5876365641%

Reaction Steps

4.22 g (10 mmol) of 2-[(2-bromo-pyridin-4-ylmethyl)-amino]-N-(1H-indazol-5-yl)-benzamide is mixed in 30 ml of dimethylformamide while being cooled with ice with 3.6 g (11 mmol) of cesium carbonate and 0.68 ml (11 mmol) of methyl iodide, and it is stirred overnight at room temperature. It is then stirred into 250 ml of ice-cold water, stirring is continued for 15 minutes, and it is suctioned off. The filter cake is quickly dried and chromatographed on silica gel with a gradient of ethyl acetate: hexane =1:1 to 100:0 as an eluant. 1.79 g (41% of theory) of 2-[(2-bromo-pyridin-4-ylmethyl)-amino]-N-(1-methyl-1H-indazol-5-yl)-benzamide with a melting point of 173.8° C. as well as 830 mg (19% of theory) of 2-[(2-bromo-pyridin-4-ylmethyl)-amino]-N-(2-methyl-2H-indazol-5-yl)-benzamide with a melting point of 183.8° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517894B2
Source datasetuspto-grants-2009_04
ORD IDord-f7f5fabf53da4387a61cee3029ce76f4
Source noteuspto-grants-2009_04