Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419739Generated: October 29, 2026

Hydrochloric Acid → HCID 66649912, compound

https://huagongshe.com/reaction/419739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1H-Pyrazolo[3,4-d]pyrimidine, 4-[4-[5-(2,4-dichlorophenyl)-1H-imidazol-2-yl]-1-piperidinyl]-HCID 66649913—
SolventMethanolHCID 887—
ProductHCID 66649912HCID 66649912129.4%

Reaction Steps

Heat a mixture of 4-(4-(2,4-dichlorophenyl)-1H-imidazol-2-yl)piperidine (270 mg, 0.91 mmol), 4-chloro-1H-pyrazolo[3,4-d]pyrimidine (280 mg, 1.82 mmol), Et3N (0.63 mL, 4.5 mmol), and 2-propanol (10 mL) at 90° C. overnight under N2. Cool the mixture to room temperature and pour into water (100 mL). Extract the mixture with CH2Cl2 (2×200 mL), combine the organic layers, and wash with water (50 mL). Dry (Na2SO4) the organic layer, filter the mixture, and concentrate the filtrate in vacuo. Purify the residue by silica gel chromatography (25 g of SiO2, elute with CH2Cl2/CMA 4:1, 1000 mL) to provide 4-(4-(5-(2,4-dichlorophenyl)-1H-imidazol-2-yl)piperidin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine (304 mg, 80%). Add hydrochloric acid (2.0 M aqueous, 0.36 mL, 0.72 mmol) to a suspension of 4-(4-(5-(2,4-dichlorophenyl)-1H-imidazol-2-yl)piperidin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine (300 mg, 0.72 mmol) in methanol (7 mL). Concentrate the mixture in vacuo to dryness. Dissolve the residue in methanol (2 mL) and add diethyl ether (50 mL) to form a precipitate. Filter the precipitate, and wash the filter cake with Et2O. Dissolve the solid in methanol (10 mL) and remove the solvent in vacuo to dryness to provide 4-(4-(5-(2,4-dichlorophenyl)-1H-imidazol-2-yl)piperidin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine hydrochloride (210 mg, 65%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093383B2
Source datasetuspto-grants-2012_01
ORD IDord-0b04ea2f6620458a969b74fe4a99ada0
Source noteuspto-grants-2012_01