Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | HCID 71623011 | HCID 71623011 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 89655910 | HCID 89655910 | — |
Reaction Steps
N-(2-cyanopropan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide (II) (185 gms) was suspended in isopropyl alcohol (462 ml), heated to 50 to 55° C. Aqueous hydroxylamine (IIIa; 76 ml) was added and the reaction mixture stirred for 30 minutes at 60° C. After completion, reaction mass was cooled between 0 and 5° C. and heptane (462 ml) was added to the reaction mass. The resultant slurry was filtered, washed with heptane (185 ml) and the wet cake was dried to give N-[(1Z)-1-amino-1-(hydroxyimino)-2-methylpropan-2-yl]-5-methyl-1,3,4-oxadiazole-2-carboxamide (IVa).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403809B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-04354564b396491f9be8942f951b8ed5 |
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| Source note | uspto-grants-2016_08 |
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