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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914354Generated: October 25, 2026

Trifluoroacetic acid → HCID 67397937, compound

https://huagongshe.com/reaction/914354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-[(4-{2-[(5-Bromopyrimidin-2-yl)amino]ethyl}-1,3-thiazol-2-yl)thio]-2-methylpropionic acid tert-butyl esterHCID 59758804—
SolventDichloromethaneHCID 6344—
ProductHCID 67397937HCID 67397937—

Reaction Steps

The compound obtained using 2-[(4-{2-[(5-bromopyrimidin-2-yl)amino]ethyl}-1,3-thiazol-2-yl)thio]-2-methylpropionic acid tert-butyl ester synthesized in Example 162-1 and phenylboronic acid as starting materials and by an operation similar to that of Example 162-2 was treated with dichloromethane and trifluoroacetic acid, and the mixture was stirred at room temperature for 12 hr. The reaction mixture was concentrated under reduced pressure, and the obtained solid was triturated and washed with hexane-ethyl acetate 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-ec967db161134fe7967b9f0598f206ed
Source noteuspto-grants-2011_09