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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914427Generated: November 2, 2026

Trifluoroacetic acid → HCID 59759199, compound

https://huagongshe.com/reaction/914427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-AminopyridineHCID 10439—
Reactant{2-[(2-Tert-butoxy-1,1-dimethyl-2-oxoethyl)thio]-1,3-thiazol-4-yl}acetic acidHCID 59759443—
SolventDichloromethaneHCID 6344—
ProductHCID 59759199HCID 59759199—

Reaction Steps

A compound obtained using {2-[(2-tert-butoxy-1,1-dimethyl-2-oxoethyl)thio]-1,3-thiazol-4-yl}acetic acid synthesized in Example 3 and 2-aminopyridine as starting materials and by an operation similar to that of Example 293-1 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=85:15 to 40:60) to give the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026370B2
Source datasetuspto-grants-2011_09
ORD IDord-77a13d8741c84ac6a931683982d8c5a9
Source noteuspto-grants-2011_09