Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 58182736 | HCID 58182736 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58182721 | HCID 58182721 | — |
Reaction Steps
A mixture of 3-chloro-5-(2-methoxyphenyl)-1,2,4-thiadiazole (0.21 g, 0.93 mmol), piperazine (400 mg, 4.65 mmol), and DMF (3 mL) was sealed in a microwave vessel and heated by microwave irradiation at 150° C. for 5 minutes. The reaction was cooled to room temperature, diluted with water, and extracted with CH2Cl2. The combined extracts were washed with water, dried over Na2SO4, and concentrated under reduced pressure to yield 1-(5-(2-methoxyphenyl)-1,2,4-thiadiazol-3-yl)piperazine. LC/MS: m/z 277.1 (M+H)+ at 2.19 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07880008B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-a8db59e350674759b7a7b33649b3957d |
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| Source note | uspto-grants-2011_02 |
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