Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 21996893 | HCID 21996893 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21996923 | HCID 21996923 | — |
Reaction Steps
20.3 g (0.0938 mol) of 4-chlorodifluoromethoxy-2,6-difluoropyrimidine were introduced into 150 ml of tetrahydrofuran and, while stirring at −70 to −60° C., 5.8 g (0.188 mol) of gaseous methylamine were added over the course of 30 minutes. The mixture was stirred for 1 hour each at −70° C., 0° C. and 25° C. and concentrated under reduced pressure. The residue was stirred with water, the mixture was extracted with ethyl acetate, and the extract was dried over magnesium sulfate. The residue from concentration under reduced pressure was chromatographed on silica gel with 5:1 petroleum ether/ether. The first fractions contained the title compound of melting point 57-61° C. in a yield of 12.5 g (58.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06235904B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-b177dcb985e64197a5e033cc67e5bedf |
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| Source note | uspto-grants-2001_05 |
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