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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827798Generated: October 30, 2026

Ammonia → HCID 22063255, compound

https://huagongshe.com/reaction/1827798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1-Pyrimidin-2-yl-piperidin-4-oneHCID 1478856—
ReactantHCID 22063255HCID 22063255—
ReactantHCID 69416907HCID 69416907—
SolventMethanolHCID 887—
ProductHCID 22063255HCID 22063255—
ProductHCID 22260486HCID 22260486—

Reaction Steps

4-Amino-4-cyano-1-pyrimidin-2-yl-piperidine was prepared according to the procedure from Example 7, step a, starting with 1-(pyrimidin-2-yl)-4-piperidone with the exception that a 2 M ammonia in methanol solution replaced the 5 M ammonia in methanol solution. (b) The title compound was prepared starting from N-(4-Morpholinecarbonyl)-L-cyclohexyl alanine and 4-amino-4-cyano-1-pyrimidin-2-yl-piperidine according to the procedure from Example 2, step b, except that the compound was purified by HPLC using a 20×250 mm C18 reverse phase column with the method being 30% acetonitrile in water to 100% acetonitrile. MS, m/z 469=M+1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056915B2
Source datasetuspto-grants-2006_06
ORD IDord-6c880bf606d44839b11252a7baebe734
Source noteuspto-grants-2006_06