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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752450Generated: October 28, 2026

Piperidin-4-ol → HCID 71283973, compound

https://huagongshe.com/reaction/1752450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-4-olHCID 79341—
ReactantHCID 89422280HCID 89422280—
SolventAcetonitrileHCID 6342—
ProductHCID 71283973HCID 71283973—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of (S)-6-((1-amino-1-oxopropan-2-yl)amino)-2-chloropyrimidine-4-carboxamide (compound 37-6) (243 mg, 1 mmol), 4-hydroxylpiperidine (101 mg, 1 mmol), and TEA (0.17 mL, 1.2 mmol) was dissolved in acetonitrile (5 mL) and stirred at 70° C. for 1 hr, extracted with EtOAc (2×20 ml), and dried over MgSO4. The ethyl acetate was removed via rotary evaporator and the crude (S)-6-((1-amino-1-oxopropan-2-yl)amino)-2-(4-hydroxypiperidin-1-yl)pyrimidine-4-carboxamide (compound 37-7) was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163008B2
Source datasetuspto-grants-2015_10
ORD IDord-295a56156d0044229bb3875347aba37e
Source noteuspto-grants-2015_10