Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfur | HCID 5362487 | — |
| Reactant | HCID 87628351 | HCID 87628351 | — |
| Reactant | (R)-(1-(5,6-diaminopyridin-2-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanone | HCID 89854052 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178521021 | HCID 178521021 | — |
Reaction Steps
1-(1H-Imidazol-1-yl)cyclopropanecarbaldehyde (60 mg, 0.44 mmol), sulfur (10 mg), and acetic acid (0.5 mL) were added to the filtrate containing (R)-(1-(5,6-diaminopyridin-2-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanone, prepared in the previous step, The reaction mixture was heated at 80° C. for 24 h. The solvent was removed under reduced pressure and the resulting crude material was purified via preparative TLC (10% methanol in dichloromethane) to afford the title compound. MS (ES+APCI) 406.1; LCMS retention time 4.739 min (Method R1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296745B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-f76168ff25aa4f4fa28e077ab00cf766 |
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| Source note | uspto-grants-2016_03 |
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