HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775153Generated: November 1, 2026
Trifluoroacetic acid → HCID 57963067, compound
https://huagongshe.com/reaction/1775153
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 6-Fluoropyridin-2-amine | HCID 2761399 | — |
| Reactant | 5-Fluoro-6-methoxypyridine-3-carbaldehyde | HCID 44754784 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57963067 | HCID 57963067 | 99% |
Reaction Steps
To 6-fluoro-pyridin-2ylamine (14, 1.50 g, 13.4 mmol) in 52.9 mL of acetonitrile, 5-fluoro-6-methoxy-pyridine-3-carbaldehyde (23, 2.00 g, 12.9 mmol), triethylsilane (10.6 mL, 66.3 mmol), and trifluoroacetic acid (5.3 mL, 69.0 mmol) were added. The reaction was stirred at 80° C. overnight, then concentrated under vacuum, combined with water 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 column chromatography, eluting with 15-100% ethyl acetate in hexane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound as white solid (24, 3.21 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260437B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-526b9c90fb334a9c8050fc1f52048c5c |
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| Source note | uspto-grants-2016_02 |
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