참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfoxide | HCID 679 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 2-Amino-4-(trifluoromethyl)benzenethiol hydrochloride | HCID 2734678 | — |
| 반응물 | 3-Fluoroisonicotinaldehyde | HCID 2763003 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-(3-Fluoropyridin-4-yl)-5-(trifluoromethyl)benzothiazole | HCID 67113761 | 60.1% |
반응 단계
A mixture of 2.3 g of 2-amino-4-(trifluoromethyl)-benzenethiol hydrochloride, 1.25 g of 3-fluoroisonicotinaldehyde, 1.29 g of N-ethyldiisopropylamine and 10 ml of DMSO was stirred for 5 hours at 170° C. The reaction mixture was cooled down to room temperature. To the reaction mixture was added water, and the resultant mixture was extracted with ethyl acetate twice. The combined organic layers were washed with water and saturated saline, dried over magnesium sulfate, then, concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, to obtain 1.79 g of 2-(3-fluoropyridin-4-yl)-5-(trifluoromethyl)benzothiazole (hereinafter, referred to as the present compound 1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08742112B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-81783412adec46318b8f5c9a7909478f |
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| 출처 메모 | uspto-grants-2014_06 |
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