Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 18180292 | HCID 18180292 | — |
| Product | HCID 9840558 | HCID 9840558 | — |
Reaction Steps
A mixture of 1-(4-chloropyrimidin-6-yl)-3-phenyl-5-(4-fluorophenyl)-1,2,4-triazine (0.080 g, 0.23 mmol) and concentrated NH4OH was heated to 120° C. for 18 h in a sealed reaction vessel. After cooling the reaction to ambient temperature, the precipitate which had formed was collected and washed with water, air-dried and dried in vacuo at 40° C. to afford the title compound as a white solid; yield 0.030 g (39%): ES MS m/z=333 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06599910B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-77e1cf3b919e4b23858a8eb497d5f74b |
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| Source note | uspto-grants-2003_07 |
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