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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409365Generated: October 30, 2026

Diisopropylcarbodiimide → HCID 70981759, compound

https://huagongshe.com/reaction/1409365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant1,5-dimethyl-1H-pyrazole-3-carboxylic acidHCID 587757—
ReactantEthyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
SolventDichloromethaneHCID 6344—
ProductHCID 70981759HCID 7098175931.9%

Reaction Steps

Ethyl aminohydroxyiminoacetate (3.78 mmol, 0.5 g), 1,5-dimethyl-1H-pyrazole-3-carboxylic acid (95%, 3.78 mmol, 0.530 g) and 1,3-diisopropylcarbodiimide (4.16 mmol, 0.525 g) were suspended in DCM (70 ml) under nitrogen atmosphere. The mixture was stirred at RT for a day. The solvent was evaporated and pyridine was added to the residue. The resulting mixture was refluxed for 6 h and stirred at RT overnight. Pyridine was evaporated and the residue diluted with DCM and water. The phases were separated and the water phase was extracted four times with DCM. The combined organics were washed with aqueous HCl solution, saturated NaHCO3, water and brine. The organic phase was dried, filtered and evaporated. The crude product was purified by flash chromatography. 0.285 g of the title compound was obtained. 1H-NMR (400 MHz, MeOH-d4): δ 1.43 (t, 3H), 2.30 (s, 3H), 4.23 (s, 3H), 4.49 (q, 2H), 6.96 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921378B2
Source datasetuspto-grants-2014_12
ORD IDord-d9cb5d0781634ae8872db7ea9b7a3914
Source noteuspto-grants-2014_12