Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 15730111 | HCID 15730111 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 15730117 | HCID 15730117 | — |
Reaction Steps
A solution of the product of Example 161 (0.9 g) in methanol (150 ml) was hydrogenated at room-temperature and pressure using 10% palladium on carbon (0.9 g) catalyst. After the uptake of hydrogen was complete, the catalyst was filtered off and the solvent evaporated. The residue was crystallised from ethanol, and gave 7-amino-2-(2-furyl)-5-[2-(hydroxyphenyl)ethyl]amino-[1,2,4]triazolo[1,5-a][1,3,5]triazine, m.p. 260°-263° C. microanalysis, found: C,57.2; H,4.8; N,28.6%; C16H15N7O2 (0.15) C2H5OH requires: C,57.0; H,4.7; N,28.5%; NMR: 2.81(t,2H, phenyl-H), 3.49(m,2H, CH2N); 6.71(d of d, 1H, furyl-4H), 7.03(d,1H, furyl-3H), 6.7-7.15 (complex, 4H, phenyl-H); 7.85(m,1H NH); 7.84(s,1H, furyl-5H); 8.09 (brs, 2H, NH2) and 9.31(s,1H, OH); m/e 338 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05270311 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-3f34a74e0d214ceaa9de2b7845ceb0e3 |
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| Source note | uspto-grants-1993_12 |
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