Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sulfamide | HCID 82267 | — |
| Reactant | HCID 69266958 | HCID 69266958 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178486298 | HCID 178486298 | 7% |
Reaction Steps
Sulfamide (32 mg, 0.33 mmol) and methylamine (15 μL, 0.33 mmol) were dissolved in pyridine (1.0 mL). The solution was heated to 120° C. for 5 minutes in a microwave. 3-[4-(aminomethyl)-1,2,5-oxadiazol-3-yl]-4-(3-chloro-4-fluorophenyl)-1,2,4-oxadiazol-5(4H)-one trifluoroacetate (32 mg, 0.075 mmol) was than added and the solution was heated to 120° C. for 3 minutes. A solution of sodium hydroxide in water (1 mL, 1 N) was added and the solution stirred at room temperature for 30 minutes. Acidification with acetic acid and purification by preparative LCMS gave the desired product (2.3 mg, 7%). MF=C11H12ClFN6O4S; LCMS calculated for C11H13ClFN6O4S (M+H)+: m/z=378.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08951536B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-81cd6ace47994517aa335107124d04c0 |
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| Source note | uspto-grants-2015_02 |
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