Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 10853541 | HCID 10853541 | — |
| Reactant | N,N-Dimethylaminoethyl chloride hydrochloride | HCID 11636816 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 20071554 | HCID 20071554 | — |
Reaction Steps
To a suspension of 5.38 g sodium hydride (0.22 mole) in 600 ml dry dimethylsulphoxide maintained at 35° C. 32.6 g 2,3-dimethyl-9-bromo-6H-indolo(2,3-b)quinoxaline (0.10 mol) is added under nitrogen and with good stirring. 30 minutes after completed addition 15.9 g N,N-dimethylamino-2-chloroethane-HCl (0.11 mole) are added at 35° C. The mixture is stirred at 35° C. for four hours and then the solvent is distilled off in vacuum at room temperature. The residue is dissolved after soaking out with water in methylacetate and slowly cooled to -30° C. whereby the base crystallizes out. Yield 22 g, 55%, mp. 146°-147° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04990510 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-b00cf8bd63de4b0f8616334dbe3dca71 |
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| Source note | uspto-grants-1991_02 |
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