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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051262Generated: October 25, 2026

2-Amino-4-(trifluoromethyl)pyridine → 1-amino-N-(2-methyl-5-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)isoquinoline-5-carboxamide

https://huagongshe.com/reaction/1051262

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-(trifluoromethyl)pyridineHCID 2778315—
Reactant1-(t-butylamino)-N-(2-methyl-5-((3-(trifluoromethyl)phenyl)carbamoyl)phenyl)isoquinoline-5-carboxamideHCID 118090796—
Product1-amino-N-(2-methyl-5-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)isoquinoline-5-carboxamideHCID 1180908187%

Reaction Steps

The procedures of Steps (1), (2) and (3) of Example 2 and Step (4) of Example 1 were repeated step by step, except for using 2-amino-4-(trifluoromethyl)pyridine instead of aniline in Step (1) of Example 2 to obtain the title compound (3.5 mg, 7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388165B2
Source datasetuspto-grants-2016_07
ORD IDord-8f65152bf78e491d97b231723a164401
Source noteuspto-grants-2016_07