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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914491Generated: November 1, 2026

Trifluoroacetic acid → HCID 67397213, compound

https://huagongshe.com/reaction/914491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-Bromobenzyl bromideHCID 68527—
Reactant6-Chloro-3-pyridinecarbonitrileHCID 5152094—
Reactant2-{[4-(2-Aminoethyl)-1,3-thiazol-2-yl]thio}-2-methylpropionic acid tert-butyl esterHCID 59759449—
SolventDichloromethaneHCID 6344—
ProductHCID 67397213HCID 67397213—

Reaction Steps

A compound obtained by an operation similar to that of Example 265-1 and using 2-{[4-(2-aminoethyl)-1,3-thiazol-2-yl]thio}-2-methylpropionic acid tert-butyl ester synthesized in Example 7 and 2-chloro-5-cyanopyridine as starting materials, followed by an operation similar to that of Example 265-2 and using 4-bromobenzylbromide as starting material was treated with dichloromethane and trifluoroacetic acid, and the mixture was stirred at room temperature for 12 hr. The reaction solution was concentrated under reduced pressure, and the residue was purified by high performance liquid chromatography (elution solvent; 0.05% trifluoroacetic acid-water:0.05% trifluoroacetic acid-acetonitrile) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026370B2
Source datasetuspto-grants-2011_09
ORD IDord-f1f42713140c44849daf50301b084799
Source noteuspto-grants-2011_09