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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528036Generated: October 25, 2026

6-chloro-N4-methylpyrimidine-4,5-diamine → 6-Chloro-8-(1-ethyl-1H-pyrazol-4-yl)-9-methyl-9H-purine

https://huagongshe.com/reaction/528036

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-chloro-N4-methylpyrimidine-4,5-diamineHCID 308477—
Reactant1-Ethyl-1H-pyrazole-4-carboxaldehydeHCID 2758900—
CatalystTrichloroiron;hexahydrateHCID 16211236—
SolventDimethylformamideHCID 6228—
Product6-Chloro-8-(1-ethyl-1H-pyrazol-4-yl)-9-methyl-9H-purineHCID 86711712103%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 6-chloro-N4-methylpyrimidine-4,5-diamine (300 mg, 1.9 mmol) in anhydrous DMF (8 mL) were added 1-ethyl-1H-pyrazole-4-carbaldehyde (236 mg, 1.9 mmol) and Iron (III) chloride hexahydrate (0.51 g, 1.9 mmol). The dark brown solution was heated to 90° C. for 14 hour in an open air vessel. The reaction mixture was cooled to room temperature and poured over ice (20 g). The resulting precipitate was collected by vacuum filtration, and triturated with 10 mL of ethanol at 50° C. for 30 min. The solids were collected by vacuum filtration to give 514 mg of the title compound. 1H NMR (400 MHz, DMSO-d6): δ 8.66 (t, 2H), 8.19 (s, 1H), 4.25 (q, 2H), 3.95 (s, 3H), 1.43 (t, 3H); MS (EI) for C11H11ClN6: 263.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346807B2
Source datasetuspto-grants-2016_05
ORD IDord-9c63682f68d14f359ca1087139334be9
Source noteuspto-grants-2016_05