HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21106545, compound → HCID 21106535, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21106545 | HCID 21106545 | — |
| Reactant | 1H-Pyrazol-3-amine, 1-(1,1-dimethylethyl)-5-methyl- | HCID 45121236 | — |
| Product | HCID 21106535 | HCID 21106535 | 31% |
Reaction Steps
4-Bromo-2-(2′-methyl-biphenyl-4-yl)-2H-phtalazin-1-one (prepared from the appropriate starting materials in analogy to Method Q-1) was coupled with 1-tert-butyl-5-methyl-1H-pyrazol-3-ylamine in a Buchwald reaction as described in Method O to give the title compound (0.049 g, 31% yield). 1H-NMR: (400 MHz, D6-DMSO) 8.44 (1H, s), 8.40 (1H, d), 8.33 (1H, d), 8.05 (1 H, t), 7.97 (1H, t), 7.62 (2H, d), 7.40 (2H, d), 7.30 (2H, d), 7.24 (2H, d), 6.00 (1H, s), 2.28 (3H, s), 2.12 (3H, s), 1.57 (9H, s); MS (ESI+)=464.36 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501410B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-0ae98676653240b38ea79251b2ab7638 |
| Source note | uspto-grants-2009_03 |