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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857661Generated: November 2, 2026

Trifluoroacetic acid → HCID 135729082, compound

https://huagongshe.com/reaction/857661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 21865184HCID 21865184—
SolventDichloromethaneHCID 6344—
ProductHCID 135729082HCID 135729082—

Reaction Steps

Trifluoroacetic acid (0.10 mL, 1.3 mmol, Aldrich) was added dropwise to a solution of N-{4-[6-(2-methoxymethoxy-4-trifluoromethyl-phenyl)-pyrimidin-4-yloxy]-benzothiazol-2-yl}-acetamide, (Example 136(b)), (0.50 g, 1.0 mmol) in dichloromethane (10 mL) with stirring and cooling in an ice bath. The reaction mixture was stirred for 16 h at room temperature, diluted with dichloromethane (5 mL) and quenched with satd sodium bicarbonate solution. The reaction mixture was diluted with water (100 mL), extracted with dichloromethane (2×100 mL), and the combined organic extracts were concentrated in vacuum. The resulting white solid was suspended in MeOH (50 mL), collected by filtration, and dried under vacuum to obtain the title compound as a white solid. Mp: 302–304° C. MS (ESI, pos. ion.) m/z: 445 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144888B2
Source datasetuspto-grants-2006_12
ORD IDord-1a758a050a65437683e36904659bf001
Source noteuspto-grants-2006_12