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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983445Generated: October 30, 2026

3-Aminobenzamide → 3-{1-[4-(3,4,5-trimethoxy-phenylamino)-[1,3,5]triazin-2-yl]-1H-benzoimidazol-2-ylamino}-benzamide

https://huagongshe.com/reaction/983445

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminobenzamideHCID 1645—
ReactantDiisopropylethylamineHCID 81531—
Reactant[4-(2-Chloro-benzimidazol-1-yl)-[1,3,5]triazin-2-yl]-(3,4,5-trimethoxy-phenyl)amineHCID 22560111—
Product3-{1-[4-(3,4,5-trimethoxy-phenylamino)-[1,3,5]triazin-2-yl]-1H-benzoimidazol-2-ylamino}-benzamideHCID 23535787—

Reaction Conditions

Temperature115 °C

Reaction Steps

A mixture of [4-(2-chloro-benzimidazol-1-yl)-[1,3,5]triazin-2-yl]-(3,4,5-trimethoxy-phenyl)amine (Example 1, step 1)(41 mg, 0.10 mmol), 3-aminobenzamide (14 mg, 0.10 mmol) and DIEA (16 mg, 0.12 mmol) in IpOH (3.5 mL) was heated at 100-130° C. for 10-40 h. On cooling a precipitate formed which was collected, washed with IpOH, ether and dried to give 3-{1-[4-(3,4,5-trimethoxy-phenylamino)-[1,3,5]triazin-2-yl]-1H-benzoimidazol-2-ylamino}-benzamide as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864255B2
Source datasetuspto-grants-2005_03
ORD IDord-bf86112d7b9b4298a3fd372765890b39
Source noteuspto-grants-2005_03