HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193349Generated: October 29, 2026
Acetyl chloride → N-Methyl-1-(pyrimidin-4-yl)piperidin-4-amine dihydrochloride
https://huagongshe.com/reaction/1193349
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | tert-Butyl methyl(1-(pyrimidin-4-yl)piperidin-4-yl)carbamate | HCID 66805510 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-Methyl-1-(pyrimidin-4-yl)piperidin-4-amine dihydrochloride | HCID 66798935 | 96% |
Reaction Steps
tert-Butyl methyl(1-(pyrimidin-4-yl)piperidin-4-yl)carbamate (3.63 mmol, 1 eq) was dissolved in ethanol (13 ml), and acetyl chloride (18.13 mmol, 5.0 eq) was added while cooling with ice. The reaction mixture was then stirred for 2 hours at 40° C. The reaction mixture was concentrated under reduced pressure. A white precipitate formed from the concentrated solution. The suspension was diluted with diethyl ether and stirred for 1 hour at RT. Then the precipitate was filtered off with suction, washed with diethyl ether and dried. Yield: 96%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680159B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-8df638d975c44ca4898e3f215499516e |
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| Source note | uspto-grants-2014_03 |
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