HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Tolylboronic acid → HCID 10362431, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Tolylboronic acid | HCID 2733950 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | HCID 21964311 | HCID 21964311 | — |
| Product | HCID 10362431 | HCID 10362431 | — |
Reaction Steps
The title compound was prepared from [1-benzyl-5-bromo-2-(hydroxymethyl)-1H-indol-3-yl](oxo)acetic acid, potassium salt and m-tolylboronic acid in substantially the same manner, as described in step 4 of Example 9. The product was obtained as a grey solid, mp: 225–226° C.; Mass spectrum (ESI, [M+H]+) m/z 382. 1H NMR (400 MHz, DMSO-d6) δ 8.22 (s, 1H), 7.22 (d, 1H, J=8.40 Hz), 7.65 (dd, 1H, J=8.45 and 1.83 Hz), 7.49 (s, 1H), 7.47–7.34 (m, 3H), 7.31 (d, 1H, J=7.33 Hz), 7.27 (d, 2H, J=8.40 Hz), 7.18 (d, 1H, J=7.48 Hz), 5.92 (s, 2H), 5.55 (s, 2H), and 2.39 ppm (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07101903B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-0e984a7f174349c2be4270ddbfcc59b0 |
| Source note | uspto-grants-2006_09 |