HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052668Generated: October 26, 2026
Water → N-(4-methyl-1-piperazinyl)-7-nitro-1,4-benzodioxane-5-carboxamide
https://huagongshe.com/reaction/2052668
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Amino-4-methylpiperazine | HCID 81349 | — |
| Reactant | 7-Nitro-1,4-benzodioxane-5-carbonyl chloride | HCID 20544745 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | N-(4-methyl-1-piperazinyl)-7-nitro-1,4-benzodioxane-5-carboxamide | HCID 20544699 | 55.8% |
Reaction Steps
33 g of 1-amino-4-methylpiperazine were dissolved in 630 ml of methyl ethyl ketone. The mixture was cooled to 10° C. and 61 g of 7-nitro-1,4-benzodioxane-5-carbonyl chloride were introduced by portions. The mixture was stirred for two hours and then the solid was filtered off and washed with 150 ml of methyl ethyl ketone. The obtained product was purified by transformation into the base (M.P.: 212° C.) and recrystallized by treatment with hydrochloric ethanol. 45 g of N-(4-methyl-1-piperazinyl)-7-nitro-1,4-benzodioxane-5-carboxamide were obtained (M.P.: 210° C. with one mole of water). The structure was confirmed by nuclear magnetic resonance and infrared analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04186135 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-0d6b2e8bffc641e787a5d73eca06e669 |
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| Source note | uspto-grants-1980_01 |
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