HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335930Generated: October 25, 2026
Dimethylformamide → (S)-4'-fluoro-7'-(2-fluoropyridin-3-yl)-2'-morpholino-5H-spiro[oxazole-4,9'-xanthen]-2-amine
https://huagongshe.com/reaction/335930
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Fluoropyridine-3-boronic acid | HCID 2783270 | — |
| Reactant | (S)-2-amino-4'-fluoro-2'-morpholino-5H-spiro[oxazole-4,9'-xanthene]-7'-yl trifluoromethanesulfonate | HCID 86658488 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-4'-fluoro-7'-(2-fluoropyridin-3-yl)-2'-morpholino-5H-spiro[oxazole-4,9'-xanthen]-2-amine | HCID 53465003 | — |
Reaction Steps
A resealable vial was charged with (S)-2-amino-4′-fluoro-2′-morpholino-5H-spiro[oxazole-4,9′-xanthene]-7′-yl trifluoromethanesulfonate (125 mg, 0.248 mmol; prepared by steps analogous to those described in Method BB40 and Example 2), tetrakis(triphenylphosphine)palladium(0) (28.7 mg, 0.025 mmol), 2-fluoropyridin-3-ylboronic acid (56.0 mg, 0.397 mmol), DMF (1.2 mL) and 2 M aqueous sodium carbonate (372 μL, 0.745 mmol). The vial was sealed and the mixture was stirred for 2 hr at 85° C. The mixture was cooled and diluted with ethyl acetate (6 mL) and water (2 ml). The organic layer was loaded onto 2 g SCX column and washed with EtOAc and MeOH/DCM 1:1. The material was recovered from the column with 2 M ammonia in MeOH, concentrated and purified by silica gel chromatography using 15-60% DCM/MeOH/NH4OH 90:10:1 in DCM to give a solid that was sonicated with 2 mL of DCM, then filtered and dried to afford (S)-4′-fluoro-7′-(2-fluoropyridin-3-yl)-2′-morpholino-5H-spiro[oxazole-4,9′-xanthen]-2-amine MS m/z=451.0 [M+H]+. Chemical Formula: C24H20F2N4O3. Exact Mass: 450.15.
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-38ad7daf5b654c25808b87178e67930a |
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| Source note | uspto-grants-2014_11 |
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