HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907567Generated: October 30, 2026
1-Phenylpiperazine → HCID 59013780, compound
https://huagongshe.com/reaction/907567
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | HCID 59013789 | HCID 59013789 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59013780 | HCID 59013780 | 9% |
Reaction Steps
4-(4-chloro-[1,2,5]thiadiazol-3-yloxymethyl)-pyridine (50 mg, 0.22 mmol) was dissolved in 200 μL of DMF along with 1-phenylpiperazine (75 μL, 0.49 mmol). The reaction was heated to 70° C. overnight. The reaction mixture was diluted with methanol to a volume of 2 mL and the reaction mixture was purified by reverse phase chromatography, affording 1-phenyl-4-{4-[(pyridin-4-ylmethyl)oxy]-1,2,5-thiadiazol-3-yl}piperazine (7 mg). 1H NMR (DMSO-d6) δ 8.62 (d, 2H), 7.46 (d, 2H), 7.23 (t, 2H), 7.01 (d, 2H), 6.82 (t, 1H), 5.58 (s, 2H), 3.64 (m, 4H), 3.23 (m, 4H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08013156B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-a06a0b0fd04e419bb727d359b1a552fc |
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| Source note | uspto-grants-2011_09 |
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