Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Amino-4-chloro-6-methylpyrimidine | HCID 21810 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(4-Hydroxymethylbenzyl)trifluoroacetamide | HCID 15852209 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 86632759 | HCID 86632759 | — |
Reaction Steps
812 mg (3.48 mmol) 2,2,2-trifluoro-N-(4-hydroxymethyl-benzyl)-acetamide is dissolved in 3 mL dry dimethylacetamide under argon atmosphere, and 167 mg (6.96 mmol) NaH is added over 5 min. 500 mg (3.48 mmol) 2-amino-4-chloro-6-methylpyrimidine is then added and the solution stirred at 90° C.— over night. 1 mL water is added carefully to quench all excess NaH, and the mixture poured into 50 ml of 0.5 N HCl. The crude product is extracted with ethyl acetate, the combined organic phases washed with brine and dried over MgSO4. After evaporation of the solvent, the product is purified by flash column chromatography (gradient ethyl acetate:cyclohexane from 1:1 to 3:1). Yield: 350 mg (29%). ESI-MS m/z 341.7 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178314B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-162dc0427521410282dfb3f6a0fbc6b3 |
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| Source note | uspto-grants-2012_05 |
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