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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685183Generated: October 25, 2026

4-chloro-5H,6H,7H-pyrrolo[2,3-d]pyrimidin-6-one → (2-{4-(4-Fluoro-3-trifluoromethyl-phenyl)-2-[1-(6-oxo-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-piperidin-4-yl]-imidazol-1-yl}-ethyl)-methyl-carbamic acid benzyl ester

https://huagongshe.com/reaction/1685183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-chloro-5H,6H,7H-pyrrolo[2,3-d]pyrimidin-6-oneHCID 12095870—
Reactant{2-[4-(4-Fluoro-3-trifluoromethyl-phenyl)-2-piperidin-4-yl-imidazol-1-yl]-ethyl}-methyl-carbamic acid benzyl ester dihydrochlorideHCID 86641608—
SolventDimethylformamideHCID 6228—
Product(2-{4-(4-Fluoro-3-trifluoromethyl-phenyl)-2-[1-(6-oxo-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-piperidin-4-yl]-imidazol-1-yl}-ethyl)-methyl-carbamic acid benzyl esterHCID 6726487179.4%

Reaction Steps

Combine {2-[4-(4-fluoro-3-trifluoromethyl-phenyl)-2-piperidin-4-yl-imidazol-1-yl]-ethyl}-methyl-carbamic acid benzyl ester dihydrochloride (277 μmol; 160 mg); 4-chloro-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-one (1.30 equiv; 360 μmol; 61.1 mg); DMF (3 mL); TEA (7 equiv; 1.94 mmol; 270 μL) and heat to 160° C. in microwave for 45 min. Evaporate, dissolve the residue in DCM, wash with saturated sodium bicarbonate and evaporate the organic layer. Purify the residue on 40 g silica gel with 3% MeOH/DCM to provide the title compound (138.2 mg; 0.22 mmol; 78%). MS (ES+): m/z=638 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148387B2
Source datasetuspto-grants-2012_04
ORD IDord-ae470a45f6f2471fb17c131fddb0238b
Source noteuspto-grants-2012_04