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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642335Generated: November 1, 2026

Cumylamine → 3-(2-Nitro-benzoylamino)-1H-furo[3,2-c]pyrazole-5-carboxylic acid (1-methyl-1-phenyl-ethyl)-amide

https://huagongshe.com/reaction/1642335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCumylamineHCID 68509—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 178507499HCID 178507499—
SolventDimethylformamideHCID 6228—
Product3-(2-Nitro-benzoylamino)-1H-furo[3,2-c]pyrazole-5-carboxylic acid (1-methyl-1-phenyl-ethyl)-amideHCID 5787864324.4%

Reaction Steps

3-(2-Amino-benzoylamino)-furo[3,2-c]pyrazole-5-carboxylic acid (11.6 g, 0.03668 mol) was dissolved in anhydrous dimethyl formamide (DMF, 70 mL). Diisopropylethylamine (DIEA, 31.4 mL, 0.1834 mol), cumylamine (7.43 mL, 0.055 mol) and 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU, 15.31 g, 0.0476 mol) were added respectively added. The solution was stirred at room temperature overnight. Then it was poured in a saturated solution of sodium bicarbonate (700 mL) and extracted with dichloromethane (2×250 ml). The organic layer was washed with water and dried over Na2SO4. The solution was then evaporated to dryness, taken up with toluene and evaporated to dryness, taken up with ethyl ether and filtered off. The solid was then purified by flash column chromatography on silica gel eluting with dichloromethane-methanol 46/4. The title compound was so obtained (3.87 g, 24.4% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119641B2
Source datasetuspto-grants-2012_02
ORD IDord-626cf8f41fc6466cab3729b2fef5caef
Source noteuspto-grants-2012_02