Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528054Generated: November 3, 2026

Hydrochloric Acid → 1'-(9-Methyl-8-pyrimidin-5-yl-9H-purin-6-yl)spiro[indole-3,4'-piperidin]-2(1H)-one

https://huagongshe.com/reaction/528054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyrimidine-5-carboxaldehydeHCID 2761034—
ReactantHCID 86711715HCID 86711715—
SolventEthanolHCID 702—
Product1'-(9-Methyl-8-pyrimidin-5-yl-9H-purin-6-yl)spiro[indole-3,4'-piperidin]-2(1H)-oneHCID 6680245328.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1′-[5-amino-6-(methylamino)pyrimidin-4-yl]spiro[indole-3,4′-piperidin]-2(1H)-one (100 mg, 0.30 mmol) in anhydrous ethanol (12 mL) were added pyrimidine-5-carbaldehyde (38 mg, 0.35 mmol, Apollo Scientific Ltd.) and catalytic amount of hydrochloric acid (0.05 mL, 4N, Dioxane, Aldrich). The reaction mixture was heated to 80° C. for 18 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The product was purified by preparatory HPLC (reverse-phase, acetonitrile/water with 0.1% formic acid) to give 35.0 mg (28% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346807B2
Source datasetuspto-grants-2016_05
ORD IDord-7cb52b0dd837471d9e75daf520266a5f
Source noteuspto-grants-2016_05