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Hydrogen Peroxide → 5-Chloro-6-((3,3-difluorocyclobutyl)methoxy)pyridin-3-OL
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrogen Peroxide | HCID 784 | — |
| 反応物 | Thiosulfite(2-) | HCID 9548651 | — |
| 反応物 | 3-Chloro-2-((3,3-difluorocyclobutyl)methoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)pyridine | HCID 58042483 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-Chloro-6-((3,3-difluorocyclobutyl)methoxy)pyridin-3-OL | HCID 58042389 | 81% |
反応手順
3-Chloro-2-[(3,3-difluorocyclobutyl)methoxy]-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (Preparation 4, 4.5 g, 12.5 mmol) was suspended in methanol (30 mL). Hydrogen peroxide (1.6 mL, 21.3 mmol) was added and the mixture stirred at room temperature under nitrogen for 16 hours. An aqueous solution of thiosulfite (10%, 10 mL) was added and the mixture was extracted with EtOAc (2×200 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (Biotage®, gradient of 0-50% EtOAc in heptane) to afford the title compound (2.53 g, 81%):
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08592629B2 |
| 出典データセット | uspto-grants-2013_11 |
| ORD ID | ord-975ab379ebe144bd9d22bd0d886a6f7e |
| 出典メモ | uspto-grants-2013_11 |