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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449371Generated: October 26, 2026

4,4,4-Trifluoro-3-methylbutanoic acid → 4-(4-Methylpiperazin-1-yl)-6-[2-(4,4,4-trifluoro-3-methylbutanoyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyrimidin-2-amine

https://huagongshe.com/reaction/449371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4,4-Trifluoro-3-methylbutanoic acidHCID 136174—
Reactant4-(4-methylpiperazin-1-yl)-6-(1,2,3,4-tetrahydroisoquinolin-7-yl)pyrimidin-2-amine HCl saltHCID 67541489—
Product4-(4-Methylpiperazin-1-yl)-6-[2-(4,4,4-trifluoro-3-methylbutanoyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyrimidin-2-amineHCID 49779587—

Reaction Steps

This compound was prepared by using procedures analogous to those described for the synthesis of Example 41 starting from 4,4,4-trifluoro-3-methylbutanoic acid (Lancaster, Cat. #L12160) and 4-(4-methylpiperazin-1-yl)-6-(1,2,3,4-tetrahydroisoquinolin-7-yl)pyrimidin-2-amine HCl salt. Analytic LCMS (M+H)+: m/z=463.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481732B2
Source datasetuspto-grants-2013_07
ORD IDord-cc4055058c284be5a486852ecf8f908c
Source noteuspto-grants-2013_07