Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | HCID 6708483 | HCID 6708483 | — |
| Reactant | HCID 86719152 | HCID 86719152 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 76071651 | HCID 76071651 | — |
Reaction Steps
3-Methyl-8-methylamino-[1,2,4]-triazolo[4,3-a]pyrazine-6-carbaldehyde (34 mg; 0.18 mmol), benzylamine (20 μl; 0.18 mmol) and 1-hydroxyimino-1-phenyl-propan-2-one (32 mg; 0.18 mmol) are dissolved in 0.6 ml acetic acid stirred for 2 h at 120° C. The reaction mixture is treated with water and extracted with DCM. The organic layer is dried over MgSO4 and evaporated to dryness. The crude intermediate is dissolved in 20 ml of THF and treated with Ra—Ni. The reaction mixture is stirred for 2 days at 25° C. and 4 bar hydrogen atmosphere. The solid materials are filtered off and the crude product is purified using reversed phase chromatography (Method: prep. HPLC1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266891B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-5e30ec331a194eadb1307dd69242d036 |
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| Source note | uspto-grants-2016_02 |
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