HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422172Generated: November 1, 2026
Trifluoroacetic anhydride → HCID 86649145, compound
https://huagongshe.com/reaction/2422172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 86649146 | HCID 86649146 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86649145 | HCID 86649145 | 100% |
Reaction Steps
To a solution of N-(4-{([5-(2-amino-2-oxoethyl)-4-chloro-6-(dimethylamino)pyrimidin-2-yl]methyl}phenyl)-2-naphthamide (0.360 g, 0.76 mmol) in pyridine (15 mL) at rt was added trifluoroacetic anhydride (0.161 mL, 1.14 mmol) dropwise and the resulting reaction mixture was stirred at room temperature for 15 hours. The volatiles were removed in vacuo and the remaining residue was partitioned between EtOAc and saturated aqueous ammonium chloride solution. The separated organic layer was washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. Purification of the resulting crude product by silica gel chromatography eluting with 20% EtOH in CHCl3 gave N-(4-{([4-chloro-5-(cyanomethyl)-6-(dimethylamino)pyrimidin-2-yl]methyl}phenyl)-2-naphthamide as an amorphous solid (0.345 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960393B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-6ab7e85e3a6544c5b71238d996a5f7b4 |
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| Source note | uspto-grants-2011_06 |
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