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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453309Generated: October 26, 2026

4-Phenylthiazole-2-carboxylic acid → N-(2-(6-((4-(2-methoxyethyl)piperazin-1-yl)methyl)thiazolo[5,4-b]pyridin-2-yl)phenyl)-4-phenylthiazole-2-carboxamide

https://huagongshe.com/reaction/453309

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenylthiazole-2-carboxylic acidHCID 3878539—
Reactant2-(6-((4-(2-Methoxyethyl)piperazin-1-yl)methyl)thiazolo[5,4-b]pyridin-2-yl)anilineHCID 58551870—
SolventWaterHCID 962—
ProductN-(2-(6-((4-(2-methoxyethyl)piperazin-1-yl)methyl)thiazolo[5,4-b]pyridin-2-yl)phenyl)-4-phenylthiazole-2-carboxamideHCID 58551890—

Reaction Steps

The title compound was prepared according to amide synthesis general method B, utilizing 2-(6-((4-(2-methoxyethyl)piperazin-1-yl)methyl)thiazolo[5,4-b]pyridin-2-yl)aniline and 4-phenylthiazole-2-carboxylic acid (1.5 eq). Addition of water to the crude reaction did not precipitate the product, therefore it was concentrated, triturated with hot MeCN, MeCN/EtOAc/MeOH mixture, and EtOAC/MeOH sequentially. The resulting pale yellow solid was lyophilized with a MeCN/water/HCl mixture and subsequently purified on prep HPLC. MS Calcd for C30H30N6O2S2: 570.19. Found (M+H)+ m/z=571.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492401B2
Source datasetuspto-grants-2013_07
ORD IDord-d52ffd5fe2024aba9b4a303aa426f200
Source noteuspto-grants-2013_07