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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Isopropoxy-4-nitrobenzoic acid | HCID 602928 | — |
| Reactant | 4-Amino-1-methylpiperidine | HCID 2737531 | — |
| Reactant | HCID 178484289 | HCID 178484289 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide | HCID 67076401 | 95.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003785B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-9a8a08cb7178483b9f4aea6a46c0219a |
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| Source note | uspto-grants-2011_08 |
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