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HRID 502556作成日:2026年10月25日

Diisopropylethylamine → HCID 58727302、化合物

https://huagongshe.com/reaction/502556

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Picolinoyl Chloride HydrochlorideHCID 135033—
反応物N1-(5-nitrobenzo[d]isothiazol-3-yl)ethane-1,2-diamineHCID 58727034—
溶媒DichloromethaneHCID 6344—
生成物HCID 58727302HCID 5872730276.6%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07776847B2
出典データセットuspto-grants-2010_08
ORD IDord-6bec3d83150b4b688d0684ec46ec3b26
出典メモuspto-grants-2010_08