Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3-Bromo-5-chloro-1,2,4-thiadiazole | HCID 2725053 | — |
| Reactant | Isobutyl piperidin-4-ylcarbamate | HCID 15676964 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58182722 | HCID 58182722 | — |
Reaction Steps
A mixture of 3-bromo-5-chloro-1,2,4-thiadiazole (0.21 g, 1.1 mmol), isobutyl piperidin-4-ylcarbamate (0.23 g, 1.2 mmol), and DMF (2 mL) was sealed in a microwave vessel and heated by microwave irradiation at 100° C. for two 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 isobutyl 1-(3-bromo-1,2,4-thiadiazol-5-yl)piperidin-4-ylcarbamate. LC/MS: m/z 365.0 (M+H)+ at 3.20 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-9c49b195cd174b98aa450fefecc71502 |
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| Source note | uspto-grants-2011_02 |
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