HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870683Generated: November 1, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 86696386, compound
https://huagongshe.com/reaction/870683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | HCID 86696383 | HCID 86696383 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86696386 | HCID 86696386 | 47% |
Reaction Steps
The reaction of the 4-(6-(butylamino)imidazo[1,2-b]pyridazin-3-yl)benzoic acid (124 mg, 0.4 mmol), tert-butyl piperazine-1-carboxylate (82 mg, 0.44 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (84 mg, 0.44 mmol) and dichloromethane (3 mL) was maintained at room temperature overnight. The resulting solution was purified by preparative HPLC (neutral) to afford tert-butyl 4-(4-(6-(butylamino)imidazo[1,2-b]pyridazin-3-yl)benzoyl)piperazine-1-carboxylate (89 mg, 47% yield) as a yellow solid: 1H NMR (METHANOL-d4) δ: 8.20-8.39 (m, J=8.3 Hz, 2H), 7.85 (s, 1H), 7.63 (d, J=9.9 Hz, 1H), 7.48-7.56 (m, 2H), 6.66-6.79 (m, 1H), 4.55 (d, J=12.1 Hz, 1H), 3.82 (br. s., 1H), 3.58-3.73 (m, 1H), 3.35-3.45 (m, 4H), 3.26 (br. s., 1H), 3.17 (d, J=15.2 Hz, 1H), 3.10 (br. s., 1H), 1.92-2.15 (m, 1H), 1.90 (br. s., 1H), 1.72 (quin, J=7.4 Hz, 2H), 1.34-1.57 (m, 14H), 1.01 (t, J=7.3 Hz, 3H); LRMS (ESI) m/e 479.3 [(M+H)+, calcd for C26H35N6O3 479.3].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969565B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-0df55dcf897248ad85bdd492e44d9488 |
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| Source note | uspto-grants-2015_03 |
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