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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1676533생성일: 2026년 10월 26일

Diisopropylethylamine → 3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide

https://huagongshe.com/reaction/1676533

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물3-Isopropoxy-4-nitrobenzoic acidHCID 602928—
반응물4-Amino-1-methylpiperidineHCID 2737531—
반응물HCID 178484289HCID 178484289—
용매DimethylformamideHCID 6228—
용매Sodium CarbonateHCID 10340—
생성물3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamideHCID 6707640195.7%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08003785B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-9a8a08cb7178483b9f4aea6a46c0219a
출처 메모uspto-grants-2011_08