HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264646Generated: October 31, 2026
Potassium Hydroxide → HCID 69419669, compound
https://huagongshe.com/reaction/1264646
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 4-[[[(7-chloro-2,3-dihydro-1,4-benzodioxin-5-yl)carbonyl]-amino]methyl]-3-methoxy-1-piperidinecarboxylate | HCID 18613663 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69419669 | HCID 69419669 | 51.8% |
Reaction Steps
A mixture of ethyl 4-[[[(7-chloro-2,3-dihydro-1,4-benzodioxin-5-yl)carbonyl]-amino]methyl]-3-methoxy-1-piperidinecarboxylate (0.051 mol) and potassium hydroxide (0.5 mol) in ethanol (200 ml) was stirred and refluxed for 30 hours and then cooled. The solvent was evaporated. The residue was dissolved in water and the solvent was evaporated again. The residue was partitioned between DCM and water. The organic layer was separated, dried, filtered, and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent : CH2Cl2/(CH3OH/NH3)93/7). The pure fractions were collected and the solvent was evaporated, yielding 9 g of (cis)-7-chloro-2,3-dihydro-N-[(3-methoxy-4-piperidinyl)methyl]-1,4-benzodioxin-5-carboxamide (interm. 3-i). Part of interm. (3-i) was dissolved in 2-propanol and converted into the ethanedioic acid salt (1:1). The precipitate was filtered off and dried, yielding 1.2 g of (cis)-7-chloro-2,3-dihydro-N-[(3-methoxy4-piperidinyl)methyl]-1,4-benzodioxin-5-carboxamide ethanedioate (1:1) (interm. 3-j, mp. 208° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06544997B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-e7882e7a78594dddb5178d1934058443 |
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| Source note | uspto-grants-2003_04 |
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