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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024198Generated: October 29, 2026

Trifluoroacetic acid → HCID 178518093, compound

https://huagongshe.com/reaction/1024198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 59593284HCID 59593284—
SolventAcetonitrileHCID 6342—
ProductHCID 178518093HCID 17851809378.3%

Reaction Conditions

Temperature85 °C

Reaction Steps

To (6-(4-chlorobenzylamino)-2-chloropyridin-3-yl)(1H-pyrrolo[2,3-b]pyridin-3-yl)methanol (P-0050, 0.028 g, 0.000070 mol) dissolved in acetonitrile (1 mL) was added triethylsilane (42.6 uL, 0.000266 mol) and trifluoroacetic acid (28.4 uL, 0.000368 mol). The reaction was heated at 85° C. overnight. The reaction was extracted with ethyl acetate and saturated sodium bicarbonate. The organic layer was separated, dried over magnesium sulfate and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with dichloromethane, 3%, 5% and finally 10% methanol in dichloromethane to give the compound as a white solid (P-0051, 20 mg, 78%). MS (ESI) [M+H+]+=365.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722702B2
Source datasetuspto-grants-2014_05
ORD IDord-78cde25b2c344e999ffc9ef4118f4b87
Source noteuspto-grants-2014_05