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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyrimidine-5-carboxaldehyde | HCID 2761034 | — |
| Reactant | HCID 86711715 | HCID 86711715 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1'-(9-Methyl-8-pyrimidin-5-yl-9H-purin-6-yl)spiro[indole-3,4'-piperidin]-2(1H)-one | HCID 66802453 | 28.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346807B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-7cb52b0dd837471d9e75daf520266a5f |
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| Source note | uspto-grants-2016_05 |
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