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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201905Generated: October 30, 2026

3-Amino-N-methylbenzamide → Ammonia

https://huagongshe.com/reaction/2201905

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 numberUS09365518B2
Source datasetuspto-grants-2016_06
ORD IDord-e5e776f01cdf4fffa43bdb0a08fc2331
Source noteuspto-grants-2016_06