참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 반응물 | 4-Heptanamine | HCID 38665 | — |
| 반응물 | Hexan-3-amine | HCID 86062 | — |
| 반응물 | HCID 86594942 | HCID 86594942 | — |
| 생성물 | HCID 86594941 | HCID 86594941 | 41% |
반응 단계
A solution of [4-chloro-5-(2-chloro-ethyl)-pyrimidin-2-yl]-(2,4,6-trimethyl-phenyl)-amine (1.3 g, 4.1 mmol) in N-methylpyrrolidinone (15 mL) was treated with 1-propyl-butylamine (1.6 g, 14 mmol) and heated to 120° C. in a sealed tube for 18 hours. Additional 1-ethyl-butylamine (0.76 g, 6.6 mmol) was added, and heating at 120° C. was resumed for 32 hours. The reaction mixture was concentrated under reduced pressure and the resulting orange solid was partitioned between ethyl acetate (100 mL) and water (100 mL). The aqueous layer was further extracted with ethyl acetate (2×75 mL), and the combined extracts were washed with 15% aqueous sodium hydroxide (2×50 mL) and brine (30 mL), dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The crude brown oil was chromatographed over silica gel, eluting with a gradient of 1 to 15% methanol in dichloromethane, to provide VII as an off-white solid (0.64 g, 41%; ESIMS m/z (M+H)=367).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07307082B2 |
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| 출처 데이터셋 | uspto-grants-2007_12 |
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| ORD ID | ord-893813ca57c548cca7e0ec165b7e0013 |
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| 출처 메모 | uspto-grants-2007_12 |
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