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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040388Generated: October 31, 2026

Trifluoroacetic acid → HCID 68500709, compound

https://huagongshe.com/reaction/2040388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68503233HCID 68503233—
SolventDichloromethaneHCID 6344—
ProductHCID 68500709HCID 68500709—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 2-(2-(2-(tert-butyldiphenylsilyloxy)ethyl)-5-(2,5-difluorophenyl)-2-phenyl-1,3,4-thiadiazol-3(2H)-yl)-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate (0.180 g, 0.226 mmol) in 4 mL of DCM at 0° C. was added TFA (1 mL). The mixture was stirred for 1 hour at 0° C. for 3 hours then concentrated in vacuo. The residue was partitioned between EtOAc (20 mL) and saturated NaHCO3 solution (20 mL) and the aqueous layer was extracted with EtOAc (2×10 mL). The combined organic phases were washed with brine (10 mL), dried over Na2SO4 and concentrated in vacuo to afford the desired product as a yellow gum, 0.157 g, 100%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580828B2
Source datasetuspto-grants-2013_11
ORD IDord-7067abae5fec41708a92168405c48db7
Source noteuspto-grants-2013_11