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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403252Generated: November 2, 2026

Trifluoroacetic acid → HCID 57963161, compound

https://huagongshe.com/reaction/1403252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
Reactant5-Iodo-6-methylpyridin-2-amineHCID 959613—
Reactant6-Methoxypyridine-3-carbaldehydeHCID 3364576—
SolventAcetonitrileHCID 6342—
ProductHCID 57963161HCID 5796316169.4%

Reaction Steps

5-Iodo-6-methyl-pyridin-2-ylamine (28, 1.7 g, 7.3 mmol) and 6-methoxy-pyridine-3-carbaldehyde (29, 1.1 g, 8.0 mmol) were combined in a round bottom flask with trifluoroacetic acid (2.80 mL, 36.3 mmol), triethylsilane (5.80 mL, 36.3 mmol) and 50 mL of acetonitrile. The reaction was stirred at room temperature overnight, then heated to reflux for 6 hours. The reaction was concentrated under vacuum, combined with aqueous potassium carbonate and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material was purified by silica gel flash column chromatography, eluting with 10-100% ethyl acetate in hexane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound (30, 1.80 g). MS (ESI)[M+H+]+=356.80.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912204B2
Source datasetuspto-grants-2014_12
ORD IDord-1c95c294af7f4d1096f8fd87e9910fd1
Source noteuspto-grants-2014_12