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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765063Generated: October 30, 2026

Dichloromethane → HCID 85418533, compound

https://huagongshe.com/reaction/1765063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant2-Furancarbonyl chlorideHCID 68242—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 21106440HCID 21106440—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 85418533HCID 854185332.3%

Reaction Steps

To a solution of 50 mg of 1-(4-{4-[3-(4-Amino-phenylamino)-[1,2,4]triazol-1-yl]-pyridin-2-yl}-2,6-dimethyl-piperazin-1-yl)-ethanone (0.123 mMol. 1.00 equiv) in 2 mL of NMP was added 5 mL of CH2Cl2 and 500 μL of Hunig's base followed by 100 μL of 2-furanoyl chloride (1.01 mMol, 8.13 equiv). The reaction mixture was stirred for 1 hr and concentrated. The resulting oil was purified via flash chromatography (EtOAc) to yield 1.4 mg of Furan-2-carboxylic acid (4-{1-[2-(4-acetyl-3,5-dimethyl-piperazin-1-yl)-pyridin-4-yl]-1H-[1,2,4]triazol-3-ylamino}-phenyl)-amide (0.0028 mMol, 2.3% yield). 1H NMR (500 MHz, MeOD-d4) ∂ 8.95 (1H, s), 8.18 (1H, d), 7.72 (1H, m), 7.61 (4H, m), 7.25 (2H, m), 7.15 (1H, m), 6.61 (1H, s), 4.30 (2H, m), 3.30 (2H, m), 3.15 (2H, m), 2.20 (3H, s), 1.35 (6H, m) ppm. LC/MS: 2.2 min/501.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226920B2
Source datasetuspto-grants-2007_06
ORD IDord-3570f54f356745f69ae47557a7a053ac
Source noteuspto-grants-2007_06