HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335769Generated: October 30, 2026
Dimethylformamide → (S)-2'-(cyclopropylethynyl)-7'-(2-methoxy-2-methylpropoxy)-5H-spiro[oxazole-4,9'-xanthen]-2-amine
https://huagongshe.com/reaction/335769
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Iodo-2-methoxy-2-methylpropane | HCID 18966832 | — |
| Reactant | (S)-2-amino-2'-(cyclopropylethynyl)-5H-spiro[oxazole-4,9'-xanthen]-7'-ol | HCID 67240959 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-2'-(cyclopropylethynyl)-7'-(2-methoxy-2-methylpropoxy)-5H-spiro[oxazole-4,9'-xanthen]-2-amine | HCID 58466161 | — |
Reaction Steps
A 2-5 mL microwave vial was charged with (S)-2-amino-2′-(cyclopropylethynyl)-5H-spiro[oxazole-4,9′-xanthen]-7′-ol (0.250 g, 0.752 mmol), cesium carbonate (0.980 g, 3.01 mmol), and DMF (3.01 mL). The mixture was stirred vigorously for 5 min, then 1-iodo-2-methoxy-2-methylpropane (0.303 mL, 2.257 mmol) was added via syringe. The vial was sealed and the reaction was microwaved at 110° C. for two hours. The mixture was diluted with water and EtOAc and the layers were separated, and the aqueous layer was extracted twice with EtOAc. The combined organic extracts were dried over sodium sulfate, filtered, and evaporated. The residue was purified by chromatography on a 12-g Redi-Sep column, eluting with 0-10% MeOH/DCM to provide (S)-2′-(cyclopropylethynyl)-7′-(2-methoxy-2-methylpropoxy)-5H-spiro[oxazole-4,9′-xanthen]-2-amine as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883782B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-829e75c3867b4877988f7abf68a58a28 |
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| Source note | uspto-grants-2014_11 |
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