참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | 6-Methoxy-4-methylpyridin-3-amine | HCID 243170 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | HCID 86717590 | HCID 86717590 | 94.6% |
반응 단계
To a 100 mL flask was added 4-methyl-6-(methyloxy)-3-pyridinamine (850 mg, 6.15 mmol), pyridine (10 mL) and then ethyl chloroformate (0.650 mL, 6.77 mmol) portionwise. The reaction mixture was stirred for 1 h at 0° C. The reaction mixture was then concentrated and partitioned between ammonium chloride and DCM, and the aqueous layer was extracted with DCM (2×). The combined organics layers were washed with brine (1×), eluted through a phase separator then concentrated to afford ethyl [4-methyl-6-(methyloxy)-3-pyridinyl]carbamate (1.223 g, 90% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09187464B2 |
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| 출처 데이터셋 | uspto-grants-2015_11 |
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| ORD ID | ord-c3e18235a1ff407ebd7487b7b56283d5 |
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| 출처 메모 | uspto-grants-2015_11 |
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