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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912866Generated: October 25, 2026

Acetic Acid → 1-[4-(6-(Methylamino)purin-9-yl)phenyl]-3-[4-(4-methylpiperazin-1-ylmethyl)-3-(trifluoromethyl)phenyl]urea

https://huagongshe.com/reaction/1912866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-MethylpiperazineHCID 53167—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(9-{4-[3-(4-formyl-3-(trifluoromethyl)phenyl)ureido]phenyl}-9H-purin-6-yl)-methylcarbamic acid tert-butyl esterHCID 59725906—
SolventEthanolHCID 702—
Product1-[4-(6-(Methylamino)purin-9-yl)phenyl]-3-[4-(4-methylpiperazin-1-ylmethyl)-3-(trifluoromethyl)phenyl]ureaHCID 2315527272.5%

Reaction Steps

In 2 mL of ethanol, 40 mg (0.07 mmol) of (9-{4-[3-(4-formyl-3-(trifluoromethyl)phenyl)ureido]phenyl}-9H-purin-6-yl)-methyl-carbamic acid tert-butyl ester was dissolved, and 15 μL of acetic acid and 20 mg (0.20 mmol) of 1-methylpiperazine were added thereto, and the mixture solution was stirred at room temperature for 30 minutes. To the reaction solution, 10 mg (0.26 mmol) of sodium cyanoborohydride was further added and the resulting solution was stirred at room temperature for one hour. The reaction solution was concentrated and partitioned between water and ethyl acetate and the organic layer was washed with a saturated sodium chloride solution, concentrated under reduced pressure and purified by a silica gel column (ethyl acetate:methanol=4:1). The obtained intermediate was dissolved in 1 mL of trifluoroacetic acid and stirred for one hour. The reaction solution was concentrated and partitioned between a saturated sodium bicarbonate solution and ethyl acetate, and the organic layer was washed with a saturated sodium chloride solution, concentrated under reduced pressure, and purified by trituration with ethyl acetate to obtain 27.4 mg (70%) of a target product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609656B2
Source datasetuspto-grants-2013_12
ORD IDord-412cf2f8d1274b77ba564af14b84cd3a
Source noteuspto-grants-2013_12