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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676533Generated: October 26, 2026

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

https://huagongshe.com/reaction/1676533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Isopropoxy-4-nitrobenzoic acidHCID 602928—
Reactant4-Amino-1-methylpiperidineHCID 2737531—
ReactantHCID 178484289HCID 178484289—
SolventDimethylformamideHCID 6228—
SolventSodium CarbonateHCID 10340—
Product3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamideHCID 6707640195.7%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003785B2
Source datasetuspto-grants-2011_08
ORD IDord-9a8a08cb7178483b9f4aea6a46c0219a
Source noteuspto-grants-2011_08