HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38800Generated: October 30, 2026
(Diethylamino)sulfur trifluoride → HCID 58168929, compound
https://huagongshe.com/reaction/38800
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 58168823 | HCID 58168823 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58168929 | HCID 58168929 | — |
Reaction Steps
To a mixture of 3-{[5-(morpholin-4-ylcarbonyl)-4-(trifluoromethyl)pyrimidin-2-yl]amino}adamantan-1-ol (150 mg) and dichloromethane (3 mL) was added diethylaminosulfur trifluoride (70 μL) under ice-cooling, followed by stirring at room temperature for 30 minutes. The reaction mixture was alkalified by adding a saturated aqueous sodium hydrogen carbonate solution, and the aqueous layer was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain N-(3-fluoroadamantan-1-yl)-5-(morpholin-4-ylcarbonyl)-4-(trifluoromethyl)pyrimidin-2-amine (115 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524727B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-9816c2136a6e41f49026b8869fbec794 |
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| Source note | uspto-grants-2013_09 |
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