참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | CID 406 | HCID 406 | — |
| 반응물 | Ketene | HCID 10038 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Diethyl (1,3-Dithian-2-yl)phosphonate | HCID 10869064 | — |
| 반응물 | 2H,3H-[1,4]dioxino[2,3-b]pyridine-6-carbaldehyde | HCID 21873786 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 촉매 | Silver Nitrate | HCID 24470 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Methyl 2-(2,3-dihydro-[1,4]dioxino[2,3-b]pyridin-6-yl)acetate | HCID 67408974 | — |
반응 단계
To a 0° C. solution of diethyl 1,3-dithian-2-ylphosphonate (12.0 g, 46.8 mmol, prepared as described in Saito, T. et al., J. Am. Chem. Soc. 1998 120 (45) 11633-11644) in THF (300 mL) was added n-BuLi (20.0 mL, 49.9 mmol, 2.5 M in hexanes) dropwise. The mixture was stirred at 0° C. for 10 minutes and was cooled to −78° C. A solution of 2,3-dihydro-[1,4]dioxino[2,3-b]pyridine-6-carbaldehyde (5.15 g, 31.2 mmol) in THF (50 mL) was added dropwise via a cannula to the phosphonate solution. The mixture was slowly warmed to room temperature over 4 hours. Saturated NH4Cl was added and the aqueous solution was washed with EtOAc. The organic solution was dried (Na2SO4) and concentrated in vacuo to provide the crude ketene dithioacetal. To a solution of the crude ketene in MeOH (400 mL) was added silver nitrate (17.2 g, 101 mmol). The reaction was heated to 60° C. overnight. The reaction was cooled to room temperature and was filtered through Celite®. The filter cake was washed with EtOAc and the filtrate was concentrated to afford methyl 2-(2,3-dihydro-[1,4]dioxino[2,3-b]pyridin-6-yl)acetate (5.50 g) which was used without further purification in the next step.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08609680B2 |
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| 출처 데이터셋 | uspto-grants-2013_12 |
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| ORD ID | ord-0a52ded3c54641b7b35186188ef42b0d |
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| 출처 메모 | uspto-grants-2013_12 |
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