HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396676Generated: November 2, 2026
Diisopropylethylamine → HCID 56928710, compound
https://huagongshe.com/reaction/1396676
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | 5-methoxy-1H,2H,3H-pyrrolo[2,3-c]pyridine | HCID 23434035 | — |
| Reactant | HCID 68018999 | HCID 68018999 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 56928710 | HCID 56928710 | 4% |
Reaction Steps
To a mixture of 106 mg of 8-fluoro-4-oxo-1-(tetrahydro-2H-pyran-4-yl)-4,5-dihydroimidazo[1,5-a]quinoxaline-7-carboxylic acid, 53 mg of 5-methoxy-2,3-dihydro-1H-pyrrolo[2,3-c]pyridine, 0.22 mL of N,N-diisopropylethylamine, and 2 mL of N,N-dimethyl formamide was added 146 mg of O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate, followed by stirring at room temperature overnight. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution, followed by extraction with chloroform. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The obtained residue was purified by preparative HPLC (methanol/0.1% aqueous formic acid solution) to obtain 5.9 mg of 8-fluoro-7-[(5-methoxy-2,3-dihydro-1H-pyrrolo[2,3-c]pyridin-1-yl)carbonyl]-1-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]quinoxalin-4(5H)-one as a pale brown 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-b5ffbd9342464375a22885f4e9fc1e00 |
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| Source note | uspto-grants-2014_12 |
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