참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | 2-Methoxypyridine | HCID 74201 | — |
| 반응물 | [2-(Methoxymethyl-carbamoyl)-ethyl]-carbamic acid tert-butyl ester | HCID 86584230 | — |
| 반응물 | HCID 178418348 | HCID 178418348 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | [4-(2-Methoxy-pyridin-3-yl)-4-oxo-butyl]-carbamic acid tert-butyl ester | HCID 102539314 | — |
반응 단계
2-Methoxypyridine (1.9 ml) and then diisopropylamine (0.1 ml) were added to a solution of methyl lithium (10 ml of a 1.6M solution in ether) in tetrahydrofuran (20 ml) at −78° C. and the solution was stirred at 0° C. for 18hand then re-cooled to −78° C. A solution of 1,1-dimethylethyl [3-(methoxymethylamino)-3-oxopropyl]-carbamate (1.6 g) in tetrahydrofuran (5 ml) was added slowly and the resultant solution was allowed to warm to −30° C. over 3.5 h, quenched with aqueous ammonium chloride and extracted with ether (three times). The combined organic extracts were dried (sodium sulphate), evaporated and purified by chromatography on silica eluting with petrol-ether gave the sub-title compound as a colourless oil (0.572 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06743939B2 |
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| 출처 데이터셋 | uspto-grants-2004_06 |
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| ORD ID | ord-3e38315d28f442a38cbf626afe239183 |
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| 출처 메모 | uspto-grants-2004_06 |
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