HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-2-amino-3-methylbutanamide → HCID 178480102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-2-amino-3-methylbutanamide | HCID 444079 | — |
| Reactant | (R)-3-((1-amino-3-methyl-1-oxobutan-2-yl)amino)-5-((1-methyl-1H-indol-4-yl)amino)-1,2,4-triazine-6-carboxamide | HCID 86706423 | — |
| Reactant | HCID 178510230 | HCID 178510230 | — |
| Product | HCID 178480102 | HCID 178480102 | — |
Reaction Steps
The title compound was prepared in a similar procedure as described in Example (R)-3-((1-amino-3-methyl-1-oxobutan-2-yl)amino)-5-((1-methyl-1H-indol-4-yl)amino)-1,2,4-triazine-6-carboxamide. Here though, 1H-Pyrazole-3-methanamine was utilized instead of (R)-2-amino-3-methylbutanamide. MS found for C17H17N9O as (M+H)+ 364.4. UV: λ=211, 239 nm. Proton NMR: (CD3OD) δ 7.90 (1H, d, J=8.0 Hz), 7.62 (1H, m), 7.34 (1H, d, J=8.8 Hz), 7.28 (1H, d, J=3.2 Hz), 7.20 (1H, t, J=8.0 Hz), 6.63 (1H, d, J=3.6 Hz), 6.33 (1H, m), 4.76 (2H, m), 3.85 (3H, s) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040530B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-37eec7ec952a47a0afaf2f2c7a855757 |
| Source note | uspto-grants-2015_05 |