Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | 6-Chloroimidazo[1,2-a]pyrazine | HCID 12841572 | — |
| Product | HCID 20299643 | HCID 20299643 | — |
Reaction Steps
6-Chloroimidazo[1,2-a]pyrazine (3.07 g, 0.020 mole) is added in portions with stirring to 20 ml chlorosulfonic acid, and the mixture heated 2 hours at 100° C. and then cooled to room temperature. Thionyl chloride (2 g) is added and the mixture reheated to 100° C. for 2 hours. After cooling to room temperature, the mixture is quenched on crushed ice and extracted with ether. The ether layer is dried over sodium sulfate, filtered and concentrated under vacuum to give an oil which is stirred with a mixture of crushed ice and aqueous dimethylamine for one hour. The crude 6-chloro-3-(N,N-dimethylsulfamoyl)imidazo[1,2-a]pyrazine is collected by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04242344 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-7c3a96f302614c9393b0c6b60f716485 |
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| Source note | uspto-grants-1980_12 |
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