HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-benzyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-Indazole → HCID 58529766, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-benzyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-Indazole | HCID 58529313 | — |
| Reactant | HCID 58529926 | HCID 58529926 | — |
| Product | HCID 58529766 | HCID 58529766 | 11% |
Reaction Steps
In a manner similar to the procedure described for step 3 of Example 83 and using 5-bromo-7-{[4-(trifluoroacetyl)piperazin-1-yl]methyl}pyrrolo[2,1-f][1,2,4]triazin-4-amine and 2-benzyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole as starting materials, 14 mg, (11%) of the desired product was isolated. 1H NMR (400 MHz, CD2Cl2) δ 8.05 (s, 1 H) 7.89 (s, 1 H) 7.74-7.81 (m, 2 H) 7.32-7.42 (m, 5 H) 7.24 (dd, 1 H) 6.71 (s, 1 H) 5.80 (br, 2 H) 5.62 (s, 2 H), 4.00 (s, 2 H) 3.59-3.71 (m, 4 H) 2.59-2.69 (m, 4 H). LC-MS [M+H]+=535.2, RT=2.51 min
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431695B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-8c5006bde5de4238b85f455006c18805 |
| Source note | uspto-grants-2013_04 |