Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiomorpholine | HCID 67164 | — |
| Reactant | HCID 10214516 | HCID 10214516 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 44409995 | HCID 44409995 | 71% |
Reaction Steps
A mixture of thiomorpholine (2.27 g, 22 mmol) and 6-chioro-N,2-dicyclopropyl-5-fluoro-4-pyrimidinamine 31 (1 g, 4.4 mmol) is stirred at 110° C. for 18 hours. After cooling, the brown solution is diluted with dichloromethane, washed two times with a saturated sodium bicarbonate solution. The combined organic layers are dried over magnesium sulfate and concentrated under high vacuum to afford a brown oil. The crude oil is purified by column chromatography (hexane/ethyl acetate: 80/20) to give N,2-dicyclopropyl-5-fluoro-6-(4-thiomorpholinyl)-4-pyrimidinamine 120 (915 mg, 71%) as a yellowish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07544675B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-2c63af0fd1c648dfbf0db312db9fb374 |
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| Source note | uspto-grants-2009_06 |
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