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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421354Generated: November 3, 2026

4-Piperidinemethanol → HCID 59333651, compound

https://huagongshe.com/reaction/421354

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PiperidinemethanolHCID 420771—
Reactant5-[8-chloro-9-(cyclopropylmethyl)-6-morpholin-4-yl-9H-purin-2-yl]-4-methylpyrimidin-2-amineHCID 59333498—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 59333651HCID 5933365158%

Reaction Conditions

Temperature120 °C

Reaction Steps

N-Methylpyrrolidone (1 ml) was added to 5-[8-chloro-9-(cyclopropylmethyl)-6-morpholin-4-yl-9H-purin-2-yl]-4-methylpyrimidin-2-amine (100 mg, 0.25 mmol) and 4-piperidinemethanol (172 mg, 1.5 mmol) and the resulting mixture was stirred at 120° C. for 0.5 hours. The reaction mixture was partitioned with ethyl acetate and water and the organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was concentrated under reduced pressure and the residue was purified by preparative HPLC (column, NOMURA Develosil Combi-RP-5; mobile phase, acetonitrile/water/formic acid) to give {1-[2-(2-amino-4-methylpyrimidin-5-yl)-9-(cyclopropylmethyl)-6-morpholin-4-yl-9H-purin-8-yl]piperidin-4-yl}methanol (69 mg, 58%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097622B2
Source datasetuspto-grants-2012_01
ORD IDord-286acaca9b454a0e8819b30bc751a984
Source noteuspto-grants-2012_01