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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237552Generated: October 31, 2026

5-Methylthiophene-2-carboxylic acid → 5-Methyl-thiophene-2-carboxylic acid (4-{2-[4-(1-methyl-piperidin-4-yl)-piperazin-1-yl]-2-oxo-ethyl}-thiazol-2-yl)-amide

https://huagongshe.com/reaction/2237552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methylthiophene-2-carboxylic acidHCID 74713—
Reactant2-(2-Amino-thiazol-4-yl)-1-[4-(1-methyl-piperidin-4-yl)-piperazin-1-yl]-ethanone trihydrobromideHCID 86606002—
Product5-Methyl-thiophene-2-carboxylic acid (4-{2-[4-(1-methyl-piperidin-4-yl)-piperazin-1-yl]-2-oxo-ethyl}-thiazol-2-yl)-amideHCID 59698868—

Reaction Steps

In analogy to example 47.3, 2-(2-amino-thiazol-4-yl)-1-[4-(1-methyl-piperidin-4-yl)-piperazin-1-yl]-ethanone trihydrobromide (example 47.2) was coupled with 5-methylthiophene-2-carboxylic acid, using general method D, to give 5-methyl-thiophene-2-carboxylic acid (4-{2-[4-(1-methyl-piperidin-4-yl)-piperazin-1-yl]-2-oxo-ethyl}-thiazol-2-yl)-amide. Light yellow solid. MS 448.4 ([M+H]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718659B2
Source datasetuspto-grants-2010_05
ORD IDord-b2efdacad0d64367a9d9fdeb1b7c0e5a
Source noteuspto-grants-2010_05