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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cumylamine | HCID 68509 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | HCID 178507499 | HCID 178507499 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(2-Nitro-benzoylamino)-1H-furo[3,2-c]pyrazole-5-carboxylic acid (1-methyl-1-phenyl-ethyl)-amide | HCID 57878643 | 24.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119641B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-626cf8f41fc6466cab3729b2fef5caef |
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| Source note | uspto-grants-2012_02 |
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