HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056112Generated: October 25, 2026
Diisopropylethylamine → HCID 89781847, compound
https://huagongshe.com/reaction/1056112
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (1-Methylcyclopropyl)amine hydrochloride | HCID 12953687 | — |
| Reactant | 1-(3-Fluoro-2-methylquinoxalin-5-yl)ethanone | HCID 89781864 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 89781847 | HCID 89781847 | — |
Reaction Steps
To a 250 mL round-bottomed flask was added 1-(3-fluoro-2-methylquinoxalin-5-yl)ethanone (126g) (14.5 g, 71 mmol), DMSO (100 mL), DIEA (27 mL, 156 mmol) and finally 1-methylcyclopropanamine hydrochloride (8.02 g, 92 mmol) (ChemBridge Corporation, San Diego, Calif.). The solution was heated at 85° C. for 7 h. After cooling to RT, the solution was poured into sat NaHCO3 (250 mL) and extracted with EtOAc (3×250 mL). The combined extracts were washed with H2O (3×250 mL) and brine and then dried (Na2SO4) and concentrated to afford 1-(2-methyl-3-((1-methylcyclopropyl)amino)-5-quinoxalinyl)ethanone (611a) as a purple solid, which was used directly in the subsequent step. m/z (ESI, +ve) 256.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394297B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-ee1526b501994188b82a1c9b466efbb3 |
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| Source note | uspto-grants-2016_07 |
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