HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403253Generated: October 31, 2026
Trifluoroacetic acid → 2-[(6-Methoxy-pyridin-3-ylmethyl)-amino]-pyrimidine-5-carbaldehyde
https://huagongshe.com/reaction/1403253
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 2-Aminopyrimidine-5-carbaldehyde | HCID 769097 | — |
| Reactant | 6-Methoxypyridine-3-carbaldehyde | HCID 3364576 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[(6-Methoxy-pyridin-3-ylmethyl)-amino]-pyrimidine-5-carbaldehyde | HCID 57963199 | — |
Reaction Steps
In a round bottom flask, 2-amino-pyrimidine-5-carbaldehyde (31, 0.750 g, 6.09 mmol), 6-methoxy-pyridine-3-carbaldehyde (29, 1.67 g, 12.2 mmol), trifluoroacetic acid (2.5 mL, 32.0 mmol), and triethylsilane (5.00 mL, 31.3 mmol) were combined with 10 mL of acetonitrile. The reaction was stirred at room temperature overnight, then concentrated under vacuum and 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 15-100% ethyl acetate in hexane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912204B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-a419b8f27fcb4fb7a4b0390cc688f53d |
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| Source note | uspto-grants-2014_12 |
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