HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050533Generated: November 1, 2026
Hydrochloric Acid → (R)-5-(3-aminopiperidin-1-yl)-3-chloropyrazine-2-carbonitrile
https://huagongshe.com/reaction/1050533
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (R)-tert-butyl 1-(6-chloro-5-cyanopyrazin-2-yl)piperidin-3-ylcarbamate | HCID 118114972 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (R)-5-(3-aminopiperidin-1-yl)-3-chloropyrazine-2-carbonitrile | HCID 118114942 | — |
Reaction Steps
(R)-tert-Butyl 1-(6-chloro-5-cyanopyrazin-2-yl)piperidin-3-ylcarbamate (87, 2.00 g, 5.93 mmol) was treated with 25 mL commercial 4N HCl in dioxane at RT for 2 hours. It was concentrated in vacuo to afford crude (R)-5-(3-aminopiperidin-1-yl)-3-chloropyrazine-2-carbonitrile (221) hydrochloride as white solid. It was dissolved in 10 mL DMF and 50 mL dioxane. To it were added DIEA (8.25 mL, 47.4 mmol) and then dropwise dimethylcarbamoyl chloride (1.64 mL, 17.8 mmol). The mixture was stirred at RT for 3 hours. It was concentrated in vacuo, diluted with 200 mL EtOAc, washed with water ×2, dried, concentrated in vacuo, subjected to silica flash column using 0 to 4% MeOH in DCM to isolate (R)-3-(1-(6-chloro-5-cyanopyrazin-2-yl)piperidin-3-yl)-1,1-dimethylurea (222) (1.47 g, 80%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382246B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-a6e2e3d88b3e4579bc1a9877e92dca8c |
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| Source note | uspto-grants-2016_07 |
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