HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754740Generated: October 26, 2026
Trifluoroacetic acid → 6-[(3-Chloro-pyridin-4-ylmethyl)-amino]-nicotinic acid methyl ester
https://huagongshe.com/reaction/1754740
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Methyl 6-aminonicotinate | HCID 737487 | — |
| Reactant | 3-Chloro-4-pyridinecarboxaldehyde | HCID 2762995 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-[(3-Chloro-pyridin-4-ylmethyl)-amino]-nicotinic acid methyl ester | HCID 57619295 | 38.6% |
Reaction Steps
To 6-amino-nicotinic acid methyl ester (553, 2.15 g, 0.014 mol) in acetonitrile (60.0 mL) were added 3-chloro-pyridine-4-carbaldehyde (554, 2.00 g, 0.014 mol), triethylsilane (11.00 mL, 0.069 mol) and trifluoroacetic acid (5.00 mL, 0.065 mol). The reaction was stirred at 80° C. overnight. The reaction was concentrated, poured into aqueous potassium carbonate, and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with 20% to 100% ethyl acetate in hexane to give the desired compound (555, 1.5 g, 38.2%). MS (ESI) [M+H+]+=278.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169250B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-62cc30febde8439a96e043aedc630090 |
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| Source note | uspto-grants-2015_10 |
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