HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261066Generated: October 27, 2026
Benzene → 6-Chloro-2-(4-cyclopropylmethyl-1-piperazinyl)-pyrazine hydrochloride
https://huagongshe.com/reaction/261066
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 6-Chloro-2-(4-cyclopropanecarbonyl-1-piperazinyl)-pyrazine | HCID 20396001 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Isopropanol ethanol | HCID 22179027 | — |
| Product | 6-Chloro-2-(4-cyclopropylmethyl-1-piperazinyl)-pyrazine hydrochloride | HCID 20396014 | — |
Reaction Steps
To a stirred slurry of 3.0 g (11 mmol) of the product from the previous step in 30 ml dry ether is added 5.5 ml of a 70% benzene solution of sodium bis-2-methoxyethoxyaluminum hydride at -20° C. under N2. The temperature of the mixture is raised to +10° C. for 20 minutes and the mixture is recooled to -20° C. and treated dropwise with 33 ml 4 N aqueous hydrochloric acid. The aqueous acid layer is extracted with chloroform, adjusted to pH8 with sodium bicarbonate and the crude title base extracted with chloroform and chromatographed on silica gel. Elution with ethylacetatechloroform gives fractions containing 0.8 g (29%) of pure title base which is converted to the hydrochloride, mp 254° C. dec in ethanol-isopropanol containing hydrochloric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04163849 |
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| Source dataset | uspto-grants-1979_08 |
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| ORD ID | ord-475abd387ef8447196e09d27c3cb3083 |
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| Source note | uspto-grants-1979_08 |
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