HuagongsheHuagongshe Chemistry Print Report · For research reference only
[2-(Benzyloxy)-5-methylphenyl]boronic acid → HCID 89544105, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | [2-(Benzyloxy)-5-methylphenyl]boronic acid | HCID 14631588 | — |
| Reactant | (5-Chloro-2-hydroxyphenyl)boronic Acid (contains varying amounts of Anhydride) | HCID 23005362 | — |
| Reactant | 5-bromo-7-(4-methoxybenzyl)imidazo[1,5-a]pyrazin-8(7H)-one | HCID 89544047 | — |
| Reactant | HCID 89544282 | HCID 89544282 | — |
| Product | HCID 89544105 | HCID 89544105 | — |
Reaction Steps
Following the procedure as described in EXAMPLE 4 and making non-critical variations to replace 5-bromo-7-(4-methoxybenzyl)imidazol[1,5-a]pyrazin-8(7H)-one with 3-benzhydryl-5-bromobenzo[d]oxazol-2(3H)-one and (5-chloro-2-hydroxyphenyl)boronic acid with (2-(benzyloxy)-5-methylphenyl)boronic acid, 3-benzhydryl-5-(2-(benzyloxy)-5-methylphenyl)benzo[d]oxazol-2(3H)-one was obtained as a colorless solid in quantitative yield (1.05 g): 1H NMR (300 MHz, CDCl3) δ7.30-7.16 (m, 17H), 6.98 (dd, J=8.3, 1.7 Hz, 1H), 6.80-6.76 (m, 3H), 6.68 (s, 1H), 4.95 (s, 2H), 2.24 (s, 3H); MS (ES+) m/z 497.8 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365578B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-01a8611199ab4a46a8d8c092dbc35830 |
| Source note | uspto-grants-2016_06 |