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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545260Generated: October 29, 2026

(5-Amino-2-(4-methylpiperazin-1-yl)phenyl)methanol → 6-{[3-hydroxymethyl-4-(4-methylpiperazin-1-yl)phenyl]amino}-2-(2-propynyl)-1-pyridin-2-yl-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

https://huagongshe.com/reaction/545260

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Amino-2-(4-methylpiperazin-1-yl)phenyl)methanolHCID 36995517—
Reactant2-allyl-6-(methylthio)-1-pyridin-2-yl-3H-pyrazolo[3,4-d]pyrimidin-3-oneHCID 67171246—
Product6-{[3-hydroxymethyl-4-(4-methylpiperazin-1-yl)phenyl]amino}-2-(2-propynyl)-1-pyridin-2-yl-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-oneHCID 86616122—

Reaction Steps

10 mg of the entitled compound was obtained as a yellow solid in the same manner as in Example 113-1 to 113-2, for which, however, 2-allyl-6-(methylthio)-1-pyridin-2-yl-3H-pyrazolo[3,4-d]pyrimidin-3-one obtained in Example 29-1 was used in place of 2-allyl-1-[6-(1-hydroxy-1-methylethyl)-2-pyridinyl]-6-(methylthio)-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one used in Example 113-1, and [5-amino-2-(4-methylpiperazin-1-yl)phenyl]methanol was used in place of 4-(4-methylpiperazin-1-yl)aniline used in Example 113-2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935708B2
Source datasetuspto-grants-2011_05
ORD IDord-35398f3a6c1844279254befc8be9b831
Source noteuspto-grants-2011_05