HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710069Generated: October 30, 2026
Dimethylformamide → (S)-1-((3-(1-(2,2-Difluoro-2-(1-hydroxy-3,3,5,5-tetramethylcyclohexyl)acetyl)pyrrolidin-2-yl)isoxazol-5-yl)methyl)pyridin-2(1H)-one
https://huagongshe.com/reaction/710069
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (S)-(3-(1-(2,2-Difluoro-2-(1-hydroxy-3,3,5,5-tetramethylcyclohexyl)acetyl)pyrrolidin-2-yl)isoxazol-5-yl)methyl methanesulfonate | HCID 86706749 | — |
| Reactant | HCID 178516071 | HCID 178516071 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (S)-1-((3-(1-(2,2-Difluoro-2-(1-hydroxy-3,3,5,5-tetramethylcyclohexyl)acetyl)pyrrolidin-2-yl)isoxazol-5-yl)methyl)pyridin-2(1H)-one | HCID 86706782 | 53.4% |
Reaction Steps
To a DMF (1.0 mL) solution of the compound (30 mg) obtained in Example 3-(5) and pyridin-2-ol (12 mg), K2CO3 (35 mg) was added and the mixture was stirred at 50° C. for an hour. To the reaction mixture, DMSO (1.0 ml) was added and after filtering off the insoluble matter, the filtrate was purified by reverse-phase preparative HPLC to give Compound 54 (2.0 mg, colorless oil) and Compound 60 (16.0 mg, colorless oil.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181229B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-aa0c01ea92134f53992c520365560fa2 |
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| Source note | uspto-grants-2015_11 |
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