HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793844Generated: November 4, 2026
Diisopropylethylamine → HCID 178512776, compound
https://huagongshe.com/reaction/1793844
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Pyrazole-1-carboxamidine monohydrochloride | HCID 2734672 | — |
| Reactant | HCID 5148325 | HCID 5148325 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178512776 | HCID 178512776 | — |
Reaction Steps
To a 2 mL pyridine solution of 5-phenylamino-[1,2,3]thiadiazole-4-carboxylic acid amide (50 mg, 0.24 mmole), was added the powder of 1H-pyrazole-1-carboxamidine hydrochloride (235 mg, 1.59 mmole) and diisopropyl ethylamine (234 mg, 1.8 mmole). Then the mixture was heated to about 80 ° C. The reaction mixture was cooled to room temperature for 4 hours and the solvent was then evaporated. The residue was loaded onto a preparative TLC plate and eluted sequentially with neat CH2Cl2 and CH2Cl2.MeOH (4:1). A 94 mg of crude product was collected, which was further purified by another preparative TLC (silica gel, CH2Cl2.MeOH.H2O=3.6:0.4:0.06). The title compound was obtained in 40 mg (66%). 1H NMR (ppm, CDCl3): 9.33 (br. t, 1 H), 8.01 (br. s, 1 H), 7.63-7.82 (m, 2 H), 7.20-7.40 (m, 3 H), 6.37 (br. s, 2 H), 6.08 (br. s, 1 H), 4.41 (d, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07022702B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-8fc5e16f7c2048f3b95aa89007d3a9e7 |
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| Source note | uspto-grants-2006_04 |
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