HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409365Generated: October 30, 2026
Diisopropylcarbodiimide → HCID 70981759, compound
https://huagongshe.com/reaction/1409365
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 1,5-dimethyl-1H-pyrazole-3-carboxylic acid | HCID 587757 | — |
| Reactant | Ethyl 2-amino-2-(hydroxyimino)acetate | HCID 6785548 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70981759 | HCID 70981759 | 31.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921378B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-d9cb5d0781634ae8872db7ea9b7a3914 |
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| Source note | uspto-grants-2014_12 |
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