참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | N-Methylisobutylamine | HCID 12249 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | Methyl 3-(hydroxymethyl)-5-methylbenzoate | HCID 21086184 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Methyl 3-{[isobutyl(methyl)amino]methyl}-5-methylbenzoate | HCID 21086186 | — |
반응 단계
To an ice-cold, stirred solution of methyl 3-(hydroxymethyl)-5-methylbenzoate (200 mg, 1.1 mmol) in methylene chloride (2.2 mL) is added triethylamine (0.304 mL, 2.2 mmol) followed by methanesulfonyl chloride (0.116 mL, 1.5 mmol). The reaction mixture is stirred for 15 min and filtered. N-Methylisobutylamine (287 mg, 3.3 mmol) is added to the filtrate, and the reaction mixture is stirred at room temperature for 5 h. The reaction mixture is diluted with methylene chloride (10 mL), washed with 1 N hydrochloric acid, and saturated sodium bicarbonate, dried (magnesium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 15% ethyl acetate/hexanes) provides the title compound. 1H NMR (300 MHz, CDCl3) δ 7.77 (s, 1H), 7.73 (s, 1H), 7.36 (s, 1H), 3.90 (s, 3H), 3.44 (s, 2H), 2.38 (s, 3H), 2.14 (s, 3H), 2.10 (d, J=8 Hz, 2H), 1.81 (m, 1H), 0.90 (d, J=7 Hz, 6H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07176242B2 |
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| 출처 데이터셋 | uspto-grants-2007_02 |
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| ORD ID | ord-3f90a1bfd7a342bc9ea6c2be329943d0 |
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| 출처 메모 | uspto-grants-2007_02 |
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