참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzamide | HCID 2331 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 6-Methyl-2-nitrobenzoic acid | HCID 16097 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | (3S,4R)-4-Amino-2,2-dimethyl-6-(trifluoromethoxy)-chroman-3-ol | HCID 15020328 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | HCID 67754289 | HCID 67754289 | 62% |
반응 단계
2-Methyl-6-nitrobenzoic acid (1.81 g, 10 mmol) was converted to the corresponding acid chloride by refluxing in benzene (30 mL) with thionyl chloride (1.66 g, 14 mmol) for 0.5 hours. The crude mixture was concentrated in vacuo and diluted with dichloromethane (10 mL). This solution was added to a cooled solution of (3S,4R)-4-amino-2,2-dimethyl-6-(trifluoromethoxy)-chroman-3-ol (2.75 g, 10 mmol), triethylamine (1.39 mL, 10 mmol) and dichloromethane (25 mL). The crude benzamide was worked-up in a method similar to that in Example 1 and chromatographed (1:1 hexanes/ethyl acetate) to afford 2.5 g (62%) of a white solid: m.p. 204°-206° C.; 1H NMR (CDCl3): δ 8.02 (d, 1H), 7.58 (d, 1H), 7.48 (t, 1H), 7.20 (s, 1H), 7.04 (d, 1H), 6.82 (d, 1 H), 6.06 (d, 1H), 3.80 (t, 1H), 3.70 (br s, 1H), 2.56 (s, 3H), 1.52 (s, 3H), 1.31 (s, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05225566 |
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| 출처 데이터셋 | uspto-grants-1993_07 |
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| ORD ID | ord-d2add3c02dae4436b92cc53ece9babf4 |
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| 출처 메모 | uspto-grants-1993_07 |
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