HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197441Generated: October 30, 2026
2-chloro-3-(morpholin-4-yl)quinoxaline → HCID 21994839, compound
https://huagongshe.com/reaction/1197441
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-chloro-3-(morpholin-4-yl)quinoxaline | HCID 240828 | — |
| Reactant | 1,2,4-Oxadiazole, 5-cyclopropyl-3-(isocyanomethyl)- | HCID 10749342 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21994839 | HCID 21994839 | — |
Reaction Steps
A solution of potassium t-butoxide (3.7 g, 32 mmol) in dry DMF (25 ml) was added to a stirred solution of 2-chloro-3-morpholino-quinoxaline (4 g, 16 mmol) and 5-cyclopropyl-3-isocyanomethyl-1,2,4-oxadiazole in dry DMF (50 ml), the temperature being kept at 0°-5° C. Then the temperature was raised to 20° C. and the solvent was evaporated in vacuo. The residue was partitioned between water (50 ml) and dichloromethane (50 ml). The organic phase was dried and evaporated and the residue was triturated with a small amount of ethyl acetate. The resulting crystalline product was collected by filtration and dried to give 3.2 g of the title compound, m.p. 169°-173° C. (Compound 9).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05276028 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-636d70258a344a2e81688b4a264a6fcf |
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| Source note | uspto-grants-1994_01 |
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