참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 3-Isopropoxy-4-nitrobenzoic acid | HCID 602928 | — |
| 반응물 | 4-Amino-1-methylpiperidine | HCID 2737531 | — |
| 반응물 | HCID 178484289 | HCID 178484289 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Sodium Carbonate | HCID 10340 | — |
| 생성물 | 3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide | HCID 67076401 | 95.7% |
반응 단계
To a mixture of 0.88 g (3.9 mmole) of 3-isopropoxy-4-nitro-benzoic acid, 2.8 mL (16 mmole) of ethyldiisopropyl amine, 0.54 g (4.7 mmole) of 4-amino-1-methyl-piperidine and 18 mL of dimethylformamide was added 1.63 g (4.3 mmole) of 1-[bis(dimethylamino)methylene)-1H-benzotriazolium 3-oxide hexafluorophosphate. The mixture was stirred at room temperature for 2 hours, then diluted with ice water and saturated sodium carbonate. The mixture was extracted with ethyl acetate 3 times. The combined organic layers were washed three times with sodium carbonate, three times with brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Purification by silica gel chromatography, eluting with dichloromethane-methanol (gradient, 100:0-40:60) gave 1.2 g of 3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide as a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08003785B2 |
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| 출처 데이터셋 | uspto-grants-2011_08 |
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| ORD ID | ord-9a8a08cb7178483b9f4aea6a46c0219a |
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| 출처 메모 | uspto-grants-2011_08 |
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