Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 68701770 | HCID 68701770 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59139820 | HCID 59139820 | — |
Reaction Steps
To a stirred solution of 2-(3-aminophenyl)-1,2,4-triazine-3,5(2H,4H)-dione (1.2 g, 5.88 mmol) in THF (20 mL) was added acetic anhydride (1.2 g, 11.8 mmol) and the mixture was heated at 50° C. After 2 h the mixture was cooled at room temperature, quenched with water and extracted with ethyl acetate (×3).The organic layers were washed with brine, dried over MgSO4, filtered and concentrated to afford the 900 mg, 62% yield, of N-(3-(3,5-dioxo-4,5-dihydro-1,2,4-triazin-2(3H)-yl)phenyl)acetamide 9(D) (900 mg, 62%) which is used in next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344138B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-345c31b02b8f43079c4f2c0d6bb67188 |
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| Source note | uspto-grants-2013_01 |
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