関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Picolinoyl Chloride Hydrochloride | HCID 135033 | — |
| 反応物 | N1-(5-nitrobenzo[d]isothiazol-3-yl)ethane-1,2-diamine | HCID 58727034 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | HCID 58727302 | HCID 58727302 | 76.6% |
反応手順
N1-(5-Nitrobenzo[d]isothiazol-3-yl)ethane-1,2-diamine (92 mg, 0.38 mmol) was dissolved in anhydrous dichloromethane (5 mL) with diisopropylethylamine (148 μL, 1.3 mmol). The solution was cooled on an ice-water bath and a solution of 2-picolinoyl chloride hydrochloride (76 mg, 2.7 mmol) in dichloromethane (0.5 mL) was added dropwise. The reaction mixture was allowed to stir for 2.5 h while warming to room temperature. The solution was diluted with dichloromethane, washed with saturated sodium bicarbonate solution, then dried over anhydrous sodium sulfate, filtered and the filtrate concentrated under reduced pressure to yield N-(2-(5-nitrobenzo[d]isothiazol-3-ylamino)ethyl)picolinamide (100 mg) as a yellow solid. 1H NMR (300 MHz, CDCl3): 8.58 (m, 1H), 8.40 (m, 1H), 8.22 (d, 1H), 7.83 (t, 1H), 7.45 (m, 2H), 7.40 (m, 2H), 3.80 (m, 2H), 3.60 ppm (m, 2H). MW=343 confirmed by LC-MS, tr=11.59 min (Method Y) MH+=344.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07776847B2 |
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| 出典データセット | uspto-grants-2010_08 |
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| ORD ID | ord-6bec3d83150b4b688d0684ec46ec3b26 |
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| 出典メモ | uspto-grants-2010_08 |
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