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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420758Generated: November 1, 2026

Furfurylamine → HCID 67214569, compound

https://huagongshe.com/reaction/2420758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfurylamineHCID 3438—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Methyl-3-{[4-(pyridin-3-yl)pyrimidin-2-yl]amino}benzoic acidHCID 10402880—
ReactantPropylphosphoric anhydrideHCID 16167369—
SolventDimethylformamideHCID 6228—
ProductHCID 67214569HCID 67214569—

Reaction Steps

A solution containing ˜50% of propylphosphonic anhydride in N,N-dimethylformamide (Fluka, Buchs, Switzerland; 674 μL, ˜1 mmol) is added within 20 minutes to a stirred mixture of 4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-benzoic acid (214.4 mg, 0.7 mmol), furfurylamine (Aldrich, Buchs, Switzerland; 61.8 μL, 0.7 mmol) and triethylamine (776 μL, 5.6 mmol) in 2 mL N,N-dimethylformamide. After stirring for 24 hours at room temperature, the mixture is treated with a half-saturated aqueous solution of sodium hydrogen carbonate and extracted three times with ethyl acetate. The solvent is evaporated off under reduced pressure and the residue dried in vacuo. The crude product is crystallised from dichloromethane to give the title compound as a crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956053B2
Source datasetuspto-grants-2011_06
ORD IDord-44c6860ef7094b35a1a76d37360597d8
Source noteuspto-grants-2011_06