HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262710Generated: November 3, 2026
Potassium Carbonate → HCID 57443120, compound
https://huagongshe.com/reaction/2262710
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | HCID 57442330 | HCID 57442330 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 57443120 | HCID 57443120 | — |
Reaction Steps
Dissolve 1-cyclobutyl-4-(piperazin-1-ylacetyl)piperazine (2.05 g, 5.46 mmol) and 3,6-dichloropyridazine (810 mg, 5.46 mmol) in dry DMSO (25 mL). Add K2CO3 (3.77 g, 27.3 mmol) and heat the mixture at 120° C. overnight. Cool and partition between CH2Cl2 (100 mL) and 1 N NaOH (150 mL). Extract the aqueous phase with CH2Cl2 (2×100 mL). Combine, dry and evaporate the organic extracts. Triturate the resulting residue with ether and filter off the solid (product). Evaporate the filtrate and chromatograph the resulting residue with EtOAc followed by EtOAc/MeOH (95:5) and EtOAc/MeOH/TEA(95:5:5) to yield additional product. 1H NMR (CDCl3) δ 7.21 (d, 1H), 6.89 (d, 1H), 3.68-3.59 (m, 8H), 3.22 (s, 2H), 2.78-2.62 (m, 5H), 2.38-2.28 (m, 4H), 2.13-2.03 (m, 2H), 1.93-1.8 (m, 2H), 1.73-1.69 (m, 2H); LC-MS (M+1) 378.98.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07851474B2 |
|---|
| Source dataset | uspto-grants-2010_12 |
|---|
| ORD ID | ord-6bf5eb30237c41a39ef64abac19e470c |
|---|
| Source note | uspto-grants-2010_12 |
|---|