HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396653Generated: November 2, 2026
Oxane-4-carboxylic acid → HCID 58575079, compound
https://huagongshe.com/reaction/1396653
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxane-4-carboxylic acid | HCID 219302 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | PyBroP | HCID 2733179 | — |
| Reactant | Methyl 3-chloro-2-hydrazino7-methylquinoxaline-6-carboxylate | HCID 86660662 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 58575079 | HCID 58575079 | 64.1% |
Reaction Steps
To a mixture of 10 g of methyl 3-chloro-2-hydrazino-7-methylquinoxaline-6-carboxylate, 5.9 g of tetrahydro-2H-pyran-4-carboxylic acid, 16 mL of triethylamine, and 100 mL of dichloromethane was added 21 g of bromo(tripyrrolidin-1-yl)phosphonium hexafluorophosphate, followed by stirring at room temperature for 9 hours. To the reaction mixture were added saturated aqueous sodium hydrogen carbonate solution and chloroform. The solid was collected by filtration and washed with ethyl acetate to obtain 9.1 g of methyl 3-chloro-7-methyl-2-[2-(tetrahydro-2H-pyran-4-ylcarbonyl)hydrazino]quinoxaline-6-carboxylate as a pink solid. Further, to the filtrate obtained above was added chloroform, and then the aqueous layer was separated. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was washed with ethyl acetate to obtain 3.58 g of methyl 3-chloro-7-methyl-2-[2-(tetrahydro-2H-pyran-4-ylcarbonyl)hydrazino]quinoxaline-6-carboxylate as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901126B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-36d5283fa38146f480eaf0fe33df2a02 |
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| Source note | uspto-grants-2014_12 |
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