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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253863Generated: November 2, 2026

3-Amino-N-methylbenzamide → Ammonia

https://huagongshe.com/reaction/1253863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-N-methylbenzamideHCID 676526—
ReactantHCID 59205709HCID 59205709—
SolventMethanolHCID 887—
ProductAmmoniaHCID 222—
ProductHCID 59205736HCID 59205736—

Reaction Conditions

Temperature60 °C

Reaction Steps

To 2-chloro-N-(5-chloroisoquinolin-6-yl) acetamide in MeOH is added KI and the solution is heated to 60° C. for 40 minutes. The mixture is cooled to 45° C. and 3-amino-N-methylbenzamide is added and stirred at 45° C. After 2-4 hours or when TLC indicates completion of the reaction, the solvents are evaporated and the residue is taken up in EtOAc and extracted with NaHCO3 (sat). The organics are dried (Na2SO4), filtered and evaporated. Flash chromatography (SiO2, NH3(2M) in MeOH/3% MeOH/CH2Cl2) gives pure 3-(2-(5-chloroisoquinolin-6-ylamino)-2-oxoethylamino)-N-methylbenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455513B2
Source datasetuspto-grants-2013_06
ORD IDord-0393f6c9ca7f4f0a9b1be855693bb32f
Source noteuspto-grants-2013_06