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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819462Generated: November 1, 2026

Benzoic Acid → HCID 178522404, compound

https://huagongshe.com/reaction/1819462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantCarbodiimideHCID 160435—
ReactantHCID 178508029HCID 178508029—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178522404HCID 17852240475%

Reaction Conditions

Temperature25 °C

Reaction Steps

N4-{[Trans-4-(3-aminoazetidin-1-yl)cyclohexyl]methyl}-5-nitro-N2-[2-(trifluoromethoxy)benzyl]pyrimidine-2,4-diamine (20 mg, 0.04 mmol) was dissolved in THF (1.0 mL). To this solution was added benzoic acid (7.3 mg, 0.06 mmol), Polystyrene-linked Carbodiimide (PS-CDI) (47 mg, 0.06 mmol) followed by triethylamine (0.084 mL, 0.06 mmol). The reaction was allowed to stir at 25° C. for 18 h. The reaction was filtered to remove the PS-CDI and the volatiles were removed in vacuo. The crude was redissolved in CH2Cl2 and extracted with 10% aqueous NaHCO3. The aqueous phase was separated and extracted two more times with CH2Cl2. The organic layers were combined, dried (Na2SO4), decanted and concentrated. The resultant residue was purified via flash chromatography (SiO2, 10-30% (2:18:80, NH4OH:CH3OH:CH2Cl2)—CH2Cl2) to afford 18 mg (74%) of the target compound, m/z 600.34 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601714B2
Source datasetuspto-grants-2009_10
ORD IDord-3d4cb4b07e714bb78d7d7831398c9ef3
Source noteuspto-grants-2009_10