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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528034Generated: October 29, 2026

1,3-Dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one → 1-(1-(8-bromo-9-methyl-9H-purin-6-yl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one

https://huagongshe.com/reaction/528034

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-oneHCID 88638—
Reactant8-Bromo-6-chloro-9-methyl-9H-purineHCID 11448012—
SolventEthanolHCID 702—
Product1-(1-(8-bromo-9-methyl-9H-purin-6-yl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-oneHCID 6680203674%

Reaction Conditions

Temperature100 °C

Reaction Steps

8-bromo-6-chloro-9-methyl-9H-purine (175 mg, 0.71 mmol) was combined with 4-(2-keto-1-benzimidazolinyl)piperidine (185 mg, 0.85 mmol) and dissolved in ethanol (2 mL). The resulting solution was warmed to 100° C. in a sealed tube for 15 minutes. A precipitate formed which was collected and washed with ethanol. An amount of 225 mg of a tan solid was isolated, which was 80% pure an indicated by LCMS analysis. A portion of this material was purified by prep HPLC to provide 6 mg of a white solid. 1H NMR (400 MHz, DMSO-d6): δ 10.80 (s, 1H), 8.21 (s, 1H), 7.14-7.00 (m, 1H), 6.88 (m, 3H), 5.38 (s, 2H), 4.48 (m, 1H), 3.62 (s, 3H), 3.13 (s, 2H), 2.25 (m, 2H), 1.78 (m, 2H). EI (MS) for C18H18BrN7O, found 428.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346807B2
Source datasetuspto-grants-2016_05
ORD IDord-92e8193a5b5643eb9f17e3039086a33d
Source noteuspto-grants-2016_05