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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424793Generated: November 1, 2026

Hydrochloric Acid → 6-[(3S,4S)-4-methylpyrrolidin-3-yl]-1-tetrahydropyran-4-yl-5H-pyrazolo[3,4-d]pyrimidin-4-one

https://huagongshe.com/reaction/2424793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPDE-9 inhibitorHCID 135886459—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product6-[(3S,4S)-4-methylpyrrolidin-3-yl]-1-tetrahydropyran-4-yl-5H-pyrazolo[3,4-d]pyrimidin-4-oneHCID 136128560103.5%

Reaction Steps

6-[(3S,4S)-1-benzyl-4-methylpyrrolidin-3-yl]-1-(tetrahydro-2H-pyran-4-yl)-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one (5.6 g) was dissolved in 100 mL of methanol and added to a Parr bottle. Palladium hydroxide (3.76 g) was added along with 3.56 mL of concentrated hydrochloric acid. The reaction mixture was placed on a hydrogenator under 40 psi of H2 for 18 h. The reaction mixture was filtered through Celite and concentrated to provide 4.47 g of the title compound as the hydrogen chloride salt. 400 MHz 1H NMR (CD3OD) δ 8.03 (s, 1H), 4.49 (m, 1H), 4.09-4.06 (m, 2H), 3.74-3.57 (m, 4H), 3.24 (m, 1H), 3.05 (m, 1H), 2.89 (m, 1H), 2.77 (m, 1H), 2.30 (m, 2H), 1.90 (m, 2H), 1.22 (d, J=6.6 Hz, 3H). MS: (M+H m/z=304.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964607B2
Source datasetuspto-grants-2011_06
ORD IDord-aa27a799581e4fdcbf1614784471872e
Source noteuspto-grants-2011_06