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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819414Generated: November 3, 2026

Benzyl Bromide → HCID 178526824, compound

https://huagongshe.com/reaction/1819414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178511544HCID 178511544—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178526824HCID 1785268246.6%

Reaction Steps

To a solution of N4-[(trans-4-aminocyclohexyl)methyl]-5-nitro-N2-[2-(trifluoromethoxy)benzyl]-pyrimidine-2,4-diamine (100 mg, 0.23 mmol) in DMF (3 mL) were added benzyl bromide (39 mg, 0.23 mmol) followed by DIPEA (40 μL, 0.23 mmol). The reaction mixture was stirred at room temperature for 20 h. The reaction mixture was diluted with EtOAc and washed with water (×4). The organic phase was dried over anhydrous Na2SO4 and concentrated in vacuo. The resulting residue was purified by silica gel prep TLC using 10:1 CH2Cl2:MeOH as an eluent to afford 8 mg of the title compound, m/z 531.6 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601714B2
Source datasetuspto-grants-2009_10
ORD IDord-f6b00996e9194568a177dd0b06b13545
Source noteuspto-grants-2009_10